Biocompatible materials containing stable complexes of tsg-6 and hyaluronan and method of using same

ABSTRACT

The present invention provides a biocompatible material in the form of a solid, a water insoluble cross-linked gel or a liposome, which contains a stable comples of TNF-stimulated gene protein (TSG-6) and hyaluronan.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims the benefit of priority from U.S.provisional application No. 61/033,204, filed Mar. 3, 2008, the entirecontent of which is hereby incorporated by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to biocompatible hyaluronan-containingmaterials and uses thereof.

2. Description of the Related Art

TNF-Stimulated Gene 6 (TSG-6)

TNF-stimulated gene 6 (TSG-6) encodes a glycoprotein of ca. 35 kDa thatis commonly referred to as TSG-6 protein (Lee et al., 1990 and 1992; andWisniewski et al., 2004). Expression and function of TSG-6 have beenassociated with inflammation and fertility.

TSG-6 protein consists of two domains, the N-terminal link module andthe C-terminal CUB domain. The N-terminal domain of TSG-6, a so-calledlink module (Kohda et al., 1996), identifies TSG-6 as a hyaluronan (HA)binding protein. All known proteins sharing this domain arehyaladherins, i.e., HA-binding proteins (Iozzo et al., 1996; Knudson etal., 1993; and Toole, 1990). Not surprisingly, TSG-6 has been shown tobind to HA in solution (Lee et al., 1992; and Kohda et al., 1992) and toimmobilized HA (Kahmann et al., 2000; Mahoney et al., 2001; Parkar etal., 1998; and Wisniewski et al., 2005). TSG-6 is the only knownHA-binding protein that contains a CUB domain, which may account forsome of its unique properties. The 3D structure of the link module ofTSG-6 has been solved and many structural details of its interactionwith HA have been investigated (Kohda et al., 1996; Kahmann et al.,2000; and Mahoney et al., 2001). The laboratory of the present inventorshave previously reported that TSG-6 formed complexes with HA covalentlyattached to a solid substrate and that these HA-TSG-6 complexes wereresistant to dissociation with guanidine HCl, guanidine HCl containinglauryl sulfobetain, SDS plus 2-mercaptoethanol, and dilute NaOH,consistent with the formation of a covalent bond (Wisniewski et al.,2005). The isolated link module is likewise competent to form thesetight complexes, indicating that the CUB domain of TSG-6 is not requiredfor this interaction with HA. The CUB domain, a modular unit that iswidely shared by numerous proteins, is thought to be a protein-proteinand protein-carbohydrate interaction domain (Bork et al., 1993; andTopfer-Petersen et al., 1998).

TSG-6 is a protein whose expression is induced by the pro-inflammatorycytokines TNF-α, IL-1 and IL-17. TSG-6 protein has shown potentanti-inflammatory and tissue-protective activities in experimentalmodels of acute and chronic inflammation. TSG-6 protein has beenparticularly impressive in ameliorating experimental arthritis, whichhas been shown in three different models of experimental arthritis usingeither recombinant TSG-6 or endogenous expression of TSG-6 in twodifferent models of transgenic mice. In addition, TSG-6-deficient micedeveloped aggravated arthritis and cartilage destruction.

TSG-6 and the ubiquitous plasma protein inter-α-inhibitor (IαI) form abiochemical pathway to permanently modify hyaluronan (HA), aglycosaminoglycan abundant in many tissues. HA is particularly prominentin joints where it serves both as a major structural component ofcartilage and, being present at high concentration in synovial fluid, aviscoelastic lubricant. TSG-6 interacts with IαI in the absence of anyother factors and serves as acceptor of one heavy chain of IαI, forminga stable TSG-6-HC complex that serves as a stable intermediate for thetransfer of HCs to hyaluronan. The resulting HA-HC complexes are stableand have been found in the synovial fluids of patients with rheumatoidarthritis and osteoarthritis (Kida et al., 1999). IαI is aprotein-polysaccharide complex of unique structure, consisting of threepolypeptide chains linked by a glycosaminoglycan (GAG) bridge (Enghildet al., 1991; and Salier et al., 1996). The smallest of the threepolypeptides, the serine protease inhibitor bikunin, carries a singlechondroitin-4-sulfate chain attached via a classical proteoglycanlinkage group, while the two closely homologous heavy chains (HC) 1 and2 are linked to hydroxyl groups of the chondroitin sulfate via esterbonds formed by their C-terminal aspartic acid residues (Enghild et al.,1989, 1991 and 1993). Purified TSG-6, in the absence of HA or any addedfactors, interacts with IαI resulting in the transfer of one HC from IαIto TSG-6 (Mukhopadhyay et al., 2004; Sanggaard et al., 2005 and 2006;and Wisniewski et al., 1994).

It is intriguing that the HCs of IαI are also found in stable complexeswith HA, and have been named serum-derived HA-associated protein (SHAP)(Huang et al., 1993). As in IαI, the HCs are coupled to HA by an esterbond formed by its C-terminal aspartic acid residue (Zhao et al., 1995).The formation of HA-HC complexes has been described both in the absence(Huang et al., 1993) or in the presence of added TSG-6 (Mukhopadhyay etal., 2004; and Rugg et al., 2005).

The HCs of IαI have also been reported to have anti-inflammatory effectsin their own right, suggested to be mediated by inhibition of complementactivation by circulating immune complexes. Activation of complement inthe vascular compartment has been associated with autoimmune andinflammatory conditions, e.g., systemic lupus erythematosus, resultingin platelet damage and fibrin deposition, both in turn causingperpetuation of inflammation.

TSG-6 has been associated with various forms of arthritis (Bayliss etal., 2001; and Wisniewski et al., 1993) and it has been demonstrated byseveral investigators to exert anti-inflammatory and chondroprotectiveeffects in murine models of acute inflammation and autoimmune arthritis(Bardos et al., 2001; Getting et al., 2002; Glant et al., 2002;Mindrescu et al., 2000 and 2002; and Wisniewski et al., 1996). TSG-6 andIαI play an essential role in female fertility, and both TSG-6- andIαI-deficient female mice are essentially infertile because theirovaries fail to form the HA-rich protective cumulus surrounding oocytesduring ovulation (Fulop et al., 2003; Sato et al., 2001; and Zhuo etal., 2001). The drop of IαI concentrations in human plasma during sepsisand the beneficial effects of exogenous IαI in experimental models ofsepsis point to a significant role of IαI in human disease (Baek et al.,2003; Balduyck et al., 2000; Lim et al., 2003; Opal et al., 2007; Wu etal., 2004; and Yang et al., 2002). Thus, IαI is considered a prognosticmarker for the outcome of septic shock in humans, with lowconcentrations of IαI predicting mortality. In experimental sepsis, IαIhas been shown to increase survival. Bikunin, the protease inhibitorychain of IαI, is also found as a free polypeptide in urine and istherefore also known as urinary trypsin inhibitor (UTI). Bikunin/UTI hasbeen described as having anti-inflammatory and anti-metastatic effectsin a range of experimental systems (Kobayashi et al., 2003 and 2006; andPugia et al., 2005).

IαI also interacts with pentraxin 3 (PTX3), a pathogen-associatedmolecular pattern receptor. This connection ties IαI firmly to theinnate immune response. PTX3 is essential for efficient innate immunityto Aspergillus fumigatus infections in the mouse. PTX3 is an activatorof complement, and its function in the innate immune system may berelated to this ability. IαI binds to PTX3 and may modulate the activityof PTX3 by its ability to modulate complement activation.

TSG-6, IαI, hyaluronan and PTX3 are collectively responsible for thestability of the expanding cumulus-oocyte complex during ovulation, andare therefore essential for female fertility. These components were alsorecently reported US2070231401 to occur in extracts of amniotic materialwith anti-inflammatory properties.

Hyaluronan

Hyaluronan is a carbohydrate polymer (polysaccharide), which is normallyfound in the matrix surrounding cells in vertebrate animals, and is amajor component of the vitreous of the eye and the synovial fluid of thejoint. Hyaluronan is synthesized by a cell surface enzyme, and extrudeddirectly into the extracellular matrix. Although some hyaluronan isdegraded locally, most is transported through the lymph and degraded inthe lymph nodes, with most of the remaining amount being cleared rapidlyfrom the blood and degraded by liver endothelial cells. Tissuehyaluronan has a rapid turnover, with approximately one-third of thetotal being degraded and replaced each day.

Commercial preparations of hyaluronan are isolated from rooster comb orfrom the culture medium of certain bacteria that are capable ofsynthesizing the polysaccharide. Hyaluronan contains two different sugarunits, which alternate in the polymer, forming a linear chain. Thenumber of sugar units in a single chain of the natural material canreach at least 40,000, which corresponds to a molecular weight of8,000,000. Commercial preparations of hyaluronan are usually lower inmolecular weight, due to degradation during isolation and purification,and are polydisperse (i.e., contain a range of molecular weights). Inreferring to the molecular weight, an average molecular weight is cited.

A large number of different biomaterials and therapeutic productscontaining hyaluronan have been proposed for use, and some have beencommercialized. Pure hyaluronan is non-immunogenic and has excellentbiocompatibility.

References for recent authoritative reviews of the chemistry, biology,and medical applications of hyaluronan are provided below (Lap{hacekover (c)}ik et al., 1998; Balazs, 2004; Asari, 2004; Miller and Avila,2004; Shu and Prestwich, 2004; Cowman and Matsuoka, 2005; Morra, 2005;Brekke and Thacker, 2006; Stern et al., 2006; Kogan et al., 2007).

Hyaluronan To Be Used In Soluble Unmodified Form

The medical applications of soluble unmodified hyaluronan include usesthat depend primarily on the physical properties (viscosity, elasticity,osmotic pressure, etc.), and uses that depend wholly or in part onbinding of hyaluronan to cell surface receptors. The molecular weight ofthe hyaluronan, and the concentration of hyaluronan in solutions, areimportant considerations in both the physical properties and the cellreceptor interactions of hyaluronan.

Physical Properties Solutions of high molecular weight (ca. 400,000 to6,000,000) hyaluronan are notable for their high viscosity and elasticcharacter, both of these depending also on the concentration and thefrequency of deformation (shear rate). Hyaluronan of lower molecularweight has much lower viscoelasticity. Hyaluronan solutions have a highosmotic pressure and contribute to tissue hydration.

Based primarily on the viscoelastic properties, solutions of highmolecular weight hyaluronan have been used extensively as tissueprotectants and manipulators (viscous tools) in ophthalmic applications,most notably cataract extraction coupled with intraocular lensimplantation. Solutions of high molecular weight hyaluronan are alsowidely used for pain relief in treatment of osteoarthritis of the knee.

Applications based primarily on the hydration properties includeprotective eye drops for treatment of dry eye, and skin moisturizers foruse in cosmetics.

Applications that depend strongly on both hydration and viscousproperties include 1) tissue protectants for use in minimizing tissueabrasion, post-surgical adhesion formation, or loss of naturalprotectant layers in peritoneal dialysis, and 2) wound protectant andhealing aids.

Solutions of high molecular weight hyaluronan at sufficiently highconcentration to have significant crowding and spatial overlap of thepolymer chains have the property of slowing the diffusion of otherco-dissolved molecules. Hyaluronan has been suggested as an adjuvant forslowed diffusion of therapeutic agents (e.g, for use in joints, wounds,ulcers, burns, etc.).

Cell Surface Receptor-Mediated Properties. Cell surface receptorinteractions may play a role in several of the above applications. It isknown that hyaluronan molecular weight influences the cell surfacereceptor interactions. High molecular weight hyaluronan, bound to thereceptors, is characteristic of the healthy physiological environment.In several pathological conditions, hyaluronan is degraded orsynthesized at a lower molecular weight. Hyaluronan with a molecularweight of less than approximately 200,000 binds to cell surfacereceptors in an altered manner, resulting in signaling that leads toexpression of genes for proteins that mediate the inflammatory response.Furthermore, small oligosaccharides (containing less than about 50sugars in a chain) of hyaluronan have still different cell signalingproperties. Oligosaccharides can induce cell death in tumor cells, maketumor cells more sensitive to chemotherapy drugs, induce blood vesselgrowth, rescue cells from inflammation, and other seemingly conflictingactivities. Each of these biological activities appears to depend on aparticular chain size. The mechanisms for these effects, and the reasonsfor the molecular weight dependence, remain to be explained in detail.Products under development include hyaluronan fragments of specificsizes.

Noncovalent Complexes of Unmodified Hyaluronan with Other Agents

A gel-like solution of the Fe³⁺ salt of hyaluronan was developed for useas an antiadhesion material in pelvic surgery, but was withdrawn. A Cu²⁺salt of hyaluronan was suggested to aid cell adhesion (Barbucci et al.,2000). Ca²⁺ was used to enhance the effect of hyaluronan in slowing thediffusion of the drug doxycycline. A mixture of hyaluronan with KI₃(which may be weakly complexed together) has been proposed for use inwound healing (Frankova et al., 2006).

Complexes of hyaluronan with positively charged drug molecules,stabilized by both electrostatic and hydrophobic interactions, weresuggested for use in drug delivery (Santos et al., 2007).

Complexes of the negatively charged hyaluronan with positively chargedpolymers (chitosan, polylysine, etc.) are generally insoluble or slowlysoluble in physiological media. The polyelectrolyte complexes have beenprepared as fibers, microspheres, surface coatings, and multilayercomposite materials. The layers can also be crosslinked into microshells(Lee et al., 2007a). The intended uses of these materials includeanti-coagulant blood vessel wall coatings to combat re-stenosis (Thierryet al., 2003a), cell culture substrates, tissue engineering scaffolds,and controlled drug release agents. Another tissue engineering matrixcomposed of hyaluronan-chitosan fibers embedded in a more solublemixture of hyaluronan and chitosan has been proposed. Hyaluronan hasalso been complexed with polypyrrole to produce an electricallyconducting material to stimulate nerve tissue regrowth. In that case,the intended role of the hyaluronan is slow degradation to releasebioactive oligosaccharides.

Insoluble or slowly soluble electrospun fibers of hyaluronan,hyaluronan/gelatin mixtures, or hyaluronan crosslinked by poly(ethyleneglycol) have been prepared for use in tissue engineering (Um et al.,2004; Li et al., 2006; Ji et al., 2006a, 2006b).

Hyaluronan can be infused into a porous three-dimensional bone graftscaffold composed of polylactic acid, to facilitate cellularinfiltration.

Soluble Chemical Derivatives of Hyaluronan

Hyaluronan can be derivatized by a number of procedures, examples ofwhich are described in the publications of Vercruysse and Prestwich,1998, Prestwich et al., 1998; Luo and Prestwich, 2001, and Shu andPrestwich, 2004.

The protein superoxide dismutase has been chemically attached tohyaluronan for use as an anti-inflammatory agent (Sakurai et al., 1997).

Chemical attachment of small molecule therapeutic agents such as

-   -   doxorubicin or other antiproliferatives (Luo and Prestwich,        1999; Rosato et al., 2006),    -   methylprednisolone or other steroid esters (Taglienti et al,        2005),    -   diclofenac or other non-steroidal anti-inflammatory agents,    -   bupivacaine or other analgesics,    -   nitric oxide for the inflammatory phase of wound healing (DiMeo        et al, 2006),    -   other therapeutic molecules        makes hyaluronan an effective pro-drug, primarily targeting the        carried drug to tumors or the liver, because these tissues have        high contents of the cell surface receptor for hyaluronan.

High molecular weight hyaluronan has been coupled withdiethylenetriamine pentaacetic acid (DTPA) (Gouin and Winnik, 2001),where the DTPA groups are used to bind radionuclides for use in cancertherapy, and the hyaluronan targets the complex to tumor cells. Lowmolecular weight hyaluronan has been coupled to DTPA to chelate Gd⁺³,and is useful as an imaging contrast agent, targeted to cell surfacereceptors in tumor tissue. Hyaluronan with attached carborane, targetedto tumor cells, may be employed as an agent in boron neutron capturetherapy (DiMeo et al, 2007).

Hyaluronan with covalently attached β-cyclodextrin molecules is able tocomplex and protect small guest molecules such as ibuprofen (Charlot etal., 2006).

Hyaluronan has been sulfated to form an anticoagulant polymer withreduced platelet attachment (Crescenzi et al, 2002).

Deacetylated hyaluronan, which is a soluble polymer with both cationic(positive) and anionic (negative) groups, bound anionic alginate to forman insoluble polyelectrolyte complex.

Attachment of lipids to hyaluronan (Dan et al., 1998; Schnitzer et al.,2000; Oohira et al., 2000; Ruhela et al., 2006) allows thepolysaccharide to be anchored in lipid bilayers, to bind low densitylipoproteins, or to affect cell behavior on substrates.

Synthetic polymers and polypeptides can be grafted onto the hyaluronanpolymer (or vice versa), providing a variety of elaborate tree-likeassemblies, with functionality based on the attached branches. Some ofthese graft copolymers are suggested for use in DNA delivery.

Hyaluronan derivatized with reactive pendant groups that can becomecrosslinked following photochemical activation have been prepared for insitu crosslinking. (see chemically crosslinked hyaluronan gels, below).

Insoluble or Slowly Soluble Derivatives of Hyaluronan

Hyaluronan fully esterified by ethyl or benzyl groups is insoluble. Thismaterial has proven to be highly biocompatible, and has beenmanufactured as anti-adhesion fabrics, sponges, membranes, skin grafts,and tissue engineering scaffolds. It is successfully used in generalsurgical applications, especially abdominal surgery, to minimizepost-operative adhesions. It is also used in repair of the tympanicmembrane of the ear, and in sinus surgery. The material may also containfibronectin or other growth factors. Tissue engineering materials may beseeded with cells.

Bioactive materials can also be built on the solid benzyl ester ofhyaluronan, coated with two types of multilayers:(poly(dimethyldiallylamonium chloride) and polystyrene sulfonate),followed by poly-D-lysine and an antibody to TGF-β1 (Pastorino et al.,2006).

Hyaluronan modified with a positively charged carbodiimide, mixed with asimilarly modified carboxymethyl cellulose, forms a polyelectrolytecomplex, in which the positively charged pendant groups and thenegatively charged carboxyl groups form electrostatic interactions. Thismaterial is successfully used as an anti-adhesion film for surgicalapplications. It is also used as a coating on polypropylene mesh forsurgical applications (see below, for surface attachment applications).

Physical Gels of Hyaluronan

Hyaluronan can form gels by an unknown mechanism, after heating andcooling procedures (Takahashi et al., 2000; Fujiwara et al., 2000). Theinter-chain associations, functionally similar to chemical crosslinks,may be aggregates that would be redissolved only over a long timeperiod.

Hydrophobic alkyl groups can be attached to hyaluronan to formamphiphilic polymers that associate strongly to form reversible physicalgels (Pelletier et al., 2000; Dausse et al., 2003; Huin-Amargier et al.,2005; Ml{hacek over (c)}ochova et al., 2006; Mrá{hacek over (c)}ek etal., 2007).

Attachment of lactic acid oligomers to a mixed salt (Na+,cetyltrimethylammonium) form of hyaluronan leads to gel formation(Pravata et al., 2008).

Host-guest interactions lead to formation of a gel when hyaluronanhaving bound β-cyclodextrin is mixed with hyaluronan having a boundacylurea. The pendant groups complex together, linking the polymerchains noncovalently ({hacek over (S)}oltés and Mendichi, 2003; {hacekover (S)}oltés et al., 2004).

Chemically Crosslinked Hyaluronan Gels

Crosslinked gels of hyaluronan have found numerous applications. Thegels may be used in the form of sieved particles, sphericalmicroparticles, membranous films, or sponges. In some cases, the gel isemployed as a long residence form of the polymer. Thus it is used inpreparations for treatment of joint pain and cartilage defects (Balazset al., 1993; Barbucci et al., 2002a; Balazs, 2004; Asari, 2004; Millerand Avila, 2004), where the turnover of soluble hyaluronan is rapid.Similarly, antiadhesion or wound dressing films formed from crosslinkedmaterial remain in place longer, with lifetimes controlled to match thephysiological need, such as medium-term prevention of post-surgicaladhesions in abdominal or nasal surgery. It can also serve a long termspace-filling function in tissue augmentation, for use in vocal foldtissue, urinary sphincter, or facial wrinkles or scars. In other cases,the main function of the gel is to serve as a reservoir of slowlyreleased hyaluronan fragments having angiogenic or chondrogenic effects.Because hyaluronan degradation is aided by reactive oxygen speciesgenerated in inflammation, the gels are plausibly termedinflammation-responsive materials.

The hyaluronan crosslinks in the gels can be created using a widevariety of chemical agents such as bisepoxides, divinylsulfone,glutaraldehyde (Crescenzi et al, 2003), carbodiimides, alkyl diamines(Barbucci et al., 2000b, 2000c, 2006), thiols, cystamine (Lee et al.,2007a), photosensitive groups, etc. as reactive species, or via theelegant Ugi and Passerini multicomponent condensations (de Nooy et al,2000). Alternatively, the hyaluronan may be treated in a manner thatresults in ester formation between carboxyl groups and alcohol groups onseparate hyaluronan chains. The hyaluronan component may be in itsnative form, or subjected to modifications such as esterification,sulfation (Barbucci et al., 2000b, 2006), oxidation of hydroxymethylgroups with subsequent esterification, attachment of functional amines(Crescenzi et al 2003), or N-deacetylation followed by modifications ofthe amino group such as sulfation (Crescenzi et al, 2002a). The gelporosity can be altered by treatment with bubbled CO₂ (Barbucci andLeone, 2004; Leone et al., 2004).

The porous hyaluronan gels can be loaded with metal ions (Giavaresi etal., 2005), drugs (Barbucci et al., 2005a), proteins, or othertherapeutic agents for slow release, resulting from inhibition of thediffusion of the added species. Tissue engineering matrices ofhyaluronan gel may be seeded with cells, or crosslinked using the facileclick-chemistry in the presence of cells (Crescenzi et al/2007).

Residual activated but incompletely reacted groups can be used tocovalently attach drugs or other agents, making the hyaluronan gel adrug carrier. In these cases, the drug release must follow degradationof the hyaluronan or cleavage of the attachment.

Crosslinked matrices of hyaluronan with collagen protein are proposedfor tissue engineering (Crescenzi et al 2002b).

In some cases, the mode of hyaluronan gel interaction with added speciescan be either simple mixture or a covalent attachment. Hyaluronan gelshave been proposed to carry cell-adhesive peptides or proteins such asantibodies, growth factors, or thrombin. They may carry enzymeinhibitors such as phospholipase A2 inhibitor or anti-inflammatoryvitamin E succinate. They may be used to provide slow release of siRNAto interfere with the synthesis of selected proteins.

Hyaluronan Attached to Surfaces

Hyaluronan-coated articles have been created to improvebiocompatibility, especially for surfaces in contact with blood, and toprovide specific desirable attributes such as lubricity, reducednonspecific protein adsorption, and reduced tissue and bacterial celladhesion (Kito and Matsuda, 1996; Hoekstra, 1999; Barbucci et al. 2003a;Morra, 2005; Taglienti et al, 2006). Specific adhesion of cellsexpressing hyaluronan receptors can also be achieved, and adhesion ofother cell types can be mediated by attachment of celladhesion-mediating peptides or proteins. The hyaluronan may bephysically coated (adsorbed) on the underlying material, or, much morecommonly, may be chemically crosslinked to it. The chemical crosslinksmay be electrostatic or covalent in nature.

Physical Attachment of Hyaluronan to Surfaces

Hyaluronan has a weak tendency to physically adsorb onto surfaces.Plastic (mostly modified polystyrene) tissue culture and microtiterplates can adsorb hyaluronan from aqueous solutions (especially, 0.1 Msodium bicarbonate) with sufficient stability that the attachments canbe exploited in assays for specific binding proteins or cells expressingthe CD44 or RHAMM receptors (Delpech et al., 1985; Goetinck et al.,1987; Barton et al., 1996; Catterall et al., 1997; Lokeshwar and Selzer,2000; Lesley et al., 2002). An important aspect of these weakattachments is the availability of the hyaluronan for specific bindinginteractions with other species. A drawback of adsorption as an approachto immobilization is the lack of long term stability. Some increase instability can be obtained if the hyaluronan is dried on the surface(Park and Tsuchiya, 2002). The same effect of drying was observed forhyaluronan adsorbed to silica that had been pretreated with oxygenplasma to add —OH groups (Khademhosseini et al., 2004; Suh et al., 2005;Fukuda et al., 2006). In the latter reports, the molecular weight of thehyaluronan was found to be an important consideration, possibly becausehigh molecular weight chains should have an increased tendency to forminteracting networks on the surface during the drying process (Cowmanand Matsuoka, 2005). Adsorption of hyaluronan to surfaces can also beexploited to form patterned surfaces, using microcontact printing ormolding approaches (Khademiosseini et al., 2004; Fukuda et al., 2006).Adsorption to silica and poly(hydroxyethyl methacrylate) was acceptable,but was poor to polystyrene unless the surface was pre-treated withoxygen plasma (Suh et al., 2004). Patterned hyaluronan on silica resistsprotein or cell adhesion, whereas bare silica sections will bindfibronectin and cells. Subsequent coating of the hyaluronan sectionswith polylysine or collagen can be employed to form adhesive surfacesfor a second cell type, thus allowing patterned co-cultures to becreated (Khademhosseini et al., 2004; Fukuda et al., 2006).

Hyaluronan can be adsorbed on a polyurethane surface that has beenpreviously coated with a gelatin layer. Photo-crosslinking of thehyaluronan layer stabilizes it for use as an anti-thrombotic coating forthe luminal surface of a narrow vascular graft (Kito and Matsuda, 1996).

Hyaluronan can be entrapped at a polyethylene surface in amicrocomposite structure for use in joint replacement implants. Thematerial is formed by allowing a silyl derivative of hyaluronan topenetrate a porous polyethylene preform, crosslinking it in place,hydrolyzing the silyl groups, adding a surface coat of hyaluronan,crosslinking that layer, and finally compressing the material tocollapse the porous structure into a hyaluronan-coated solid withexcellent wear properties (Zhang et al., 2006, 2007).

Covalent Attachment of Hyaluronan to Metallic Surfaces

Stable immobilization of hyaluronan on surfaces is achieved by covalentattachment of the polysaccharide, either directly to the surface, or viaattachment to a bridging adhesive polymer layer.

Metal substrates (stainless steel, nickel titanium, titanium) are ofinterest, with respect to medical uses as stents, guide wires, dentaland orthopedic implants, sensors, or other devices. The strategy forattachment of hyaluronan is to generate functional groups on the metalsurface, and then employ appropriate chemistry to link the hyaluronanmolecules.

Functional group generation on metal surfaces can be achieved by methodssuch as 1) formation of an oxide layer on the metal surface, thenreaction with a functional silane derivative (U.S. Pat. No. 5,356,433;U.S. Pat. No. 5,336,518; Pitt et al., 2003); 2) plasma treatment in thepresence of air, argon, acetaldehyde, allylamine,hexafluorobutylmethacrylate, etc., to generate groups such as aldehdydesand amines on the metal surface (U.S. Pat. No. 5,356,433; U.S. Pat. No.5,336,518; Thierry et al., 2004; Morra et al., 2006); 3) dip coatingwith an adhesive acrylic polymer bearing isocyanate groups (U.S. Pat.No. 5,037,677); 4) dip coating with polyethyleneimine having free aminegroups (Thierry et al., 2003b); 5) dip coating with dopamine to form anadhesive polymer layer having quinone-like properties (Lee et al.,2007b).

The covalent attachment of hyaluronan to these modified surfaces can beachieved by approaches such as 1) reaction with surface amine groups viacarbodiimide activation of hyaluronan carboxyl groups (Larsson, 1987;U.S. Pat. No. 5,356,433; U.S. Pat. No. 5,336,518; Thierry et al., 2004;Morra et al., 2006); 2) reaction of surface amines with the reducing endaldehyde function of short hyaluronan chains to form a Schiff base whichis subsequently reduced (U.S. Pat. Nos. 4,613,665 and 4,810,784); 3)reaction of surface aldehyde groups with an adipic dihydrazidederivative of hyaluronan (Pitt et al., 2003); 4) urethane link formationbetween surface isocyanate groups and hydroxyl groups of hyaluronan(U.S. Pat. No. 5,037,677); 5) attachment of surface quinone-like groupsof polydopamine with thiol or amine derivatives of hyaluronan (Lee etal., 2007a).

The hyaluronan-derivatized metal surfaces can differ in the degree towhich the hyaluronan can bind proteins, cells, etc. The surfaces aregenerally intended to be resistant to nonspecific adsorption of proteinsor cells. There is special interest in surfaces that do not bindfibrinogen or platelets. Cells expressing CD44 can adhere to somesurfaces. There is currently insufficient knowledge about the bestapproaches to control the frequency of hyaluronan attachments to thesurface, and thus control the degree to which the surface-boundhyaluronan is available to show specific binding interactions withproteins or cells.

One special metallic surface that is easily and specifically reacted forattachment of hyaluronan is gold. Gold nanoparticles were reacted withhyaluronan bearing thiol groups, previously attached via carbodiimideactivation of carboxyl groups and coupling to cystamine, followed byreduction of the pendant disulfide to a thiol (Lee et al., 2006). Manysmall nanoparticles could be linked to a single long polymer ofhyaluronan, resulting in a necklace of gold nanoparticles.

Covalent Attachment of Hyaluronan to Polymeric Surfaces

Attachment of hyaluronan to polymeric substrates has also been widelyinvestigated for use in implants, catheters, etc. Among the polymericsubstrates investigated for hyaluronan attachment are polystyrene,poly(methyl methacrylate), silicone rubber, poly(tetrafluoroethylene)[Teflon], poly(ethylene terephthalate), polyurethane, poly(vinylalcohol), polyethylene, and polypropylene. There are patents dating fromthe mid 80's on hyaluronan-modified polymers (e.g., Balazs, Leschiner,and coworkers patents 1984, 1985; Beavers and Halpern patents 1987,1989, 1991; Larm patents 1986, 1989). There are a number of strategiesused to form stable covalent attachments of hyaluronan to surfaces.

The polymer surface may be treated with a plasma to provide appropriatefunctional groups such as amines. For example, commercially availableaminated polystyrene materials may be reacted with carbodiimideactivated hyaluronan (Frost and Stern, 1997) or reacted first with anazide-bearing group then photocrosslinked to hyaluronan (Joester et al.,2006). Ammonia plasma treatment can be used to aminate the surface priorto photo-immobilization of an azidophenyl hyaluronan derivative(Barbucci et al., 2005b). Ammonia plasma treatment followed by reactionwith succinic anhydride produces surface carboxyl groups that can bereacted with an adipic hydrazide derivative of hyaluronan (Mason et al.,2000). The surface can be activated by air plasma treatment, reactionwith polyethyleneimine, and subsequently reacted withcarbodiimide-activated hyaluronan (Morra and Cassinelli, 1999;Cassinelli et al., 2000). The substrate may be activated by plasmapolymerization of acetaldehyde, then Schiff base formation withpoly(allylamine), followed by reaction with carbodiimide-activatedhyaluronan (Thierry et al., 2004).

Poly(ethylene terephthalate) can be oxidized in base at high temperatureto form carboxyl groups, then coated with a cationic polymer prior tohyaluronan (Liu et al., 2006).

Hyaluronan can be photochemically immobilized on silicone rubber, afterinitial immobilization of a polyacrylamide layer, then a hyaluronanlayer, both linked covalently using the 4-benzoyl benzoic acidderivatives (DeFife et al., 1999). Hyaluronan can also be covalentlyattached to more adhesive polymer layers that are strongly attached tothe substrate. Coating PMMA with an acrylic polymer bearing isocyanatescan be used to attach hyaluronan via urethane linkages to its hydroxylgroups (Lowry and Beavers, 1994; U.S. Pat. Nos. 4,663,233; 4,801,475;and 5,037,677). Dopamine coating on polymeric surfaces leads to apolymeric coating containing quinone-like groups to which thiol oramine-derivatized hyaluronan can attach (Lee et al., 2007b).

As for the attachment of hyaluronan to metallic surfaces, the frequencyof attachment points of the hyaluronan molecule to polymeric surfacescan affect its ability to interact with proteins or cells. Whenattachment points are closely spaced, the hyaluronan can be resistant todegradation by hyaluronidase, and thus show long term stability (Lowryand Beavers, 1994). In most published studies, hyaluronan-coated polymermaterials are reported to be anti-adhesive to most proteins and cells,but show specific adhesion of CD44+ cells.

Covalent Attachment of Hyaluronan to Silica Surfaces

Hyaluronan can be covalently attached to glass (silica). Applications ofthe coated silica are primarily in cell culture. Many silica surfacesmodified with hyaluronan are notable for inhibiting cell adhesion.

Most of the silica-based surfaces are derivatized via silane chemistry.If the silica is reacted with an aminosilane which becomes covalentlyattached as a monolayer presenting amino groups, then hyaluronan thathas an azidophenyl group can be photo-immobilized and evenmicropatterned on the surface using a photolithographic mask procedure(Barbucci et al., 2003; Chiumiento et al., 2007). A surface bearingaminosilanes can also be reacted with carboxyl groups of hyaluronan viacarbodiimide coupling (Albersdörfer and Sackmann, 1999; Ibrahim et al.,2007; Joddar et al., 2007). Fluoroalkylsilanes on silica can bephoto-crosslinked with hyaluronan bearing azidoaryl groups (Wang et al.,2006). Chlorotrimethylsilane on silica provides a hydrophobic surfacethat can adhere to poly(lactic-co-glycolic acid), allowing subsequentcoating with polyethyleneimine and finally attachment of hyaluronan bycarbodiimide chemistry (Croll et al., 2006). It is also possible to makea silane-bearing derivative of hyaluronan, which can directly react withthe bare silica surface (Pasqui et al., 2007). This latter method may bepreferred because fewer of the hyaluronan carboxyl groups arederivatized, and therefore remain able to participate in hyaluronaninteractions with other species such as proteins. Hyaluronan attached tosilica by these procedures does not promote cell adhesion (Barbucci etal. 2003b; 2005b; Pasqui et al., 2007; Chiumiento et al., 2007).

An alternative approach to silica surface modification is the use of anethylene plasma to create a hydrophobic surface, oxidation of that layerin an air plasma, followed by coating with polyethyleneimine. The aminegroups can then be reacted with hyaluronan carboxyl groups viacarbodiimide chemistry (Morra et al., 2003).

Covalent Attachment of Hyaluronan to Quantum Dots

Quantum dots of CdSe/ZnS, with attached ligands containing terminalcarboxyl groups, have been derivatized by carbodiimide-mediated reactionwith amine groups on an adipic acid dihydrazide derivative of hyaluronan(Kim et al., 2008).

Electrostatic Attachment of Hyaluronan to Surfaces

Electrostatic immobilization of hyaluronan has also been widelyinvestigated. A metal or silica surface may be precoated with cationicpolymers such as polyethyleneimine, chitosan, or polylysine prior toelectrostatic attachment of hyaluronan (Morra et al., 2003; Burke andBarrett, 2003; Thierry et al. 2003b; Hahn and Hoffman, 2005; Tezcaner etal., 2006). Gold-coated silica substrate can be reacted withcarboxylated alkylthiols to form an anionic monolayer, coated withcationic polyethyleneimine, and then electrostatically linked tohyaluronan (Kujawa et al., 2005). Nanospheres of poly-ε-caprolactone canbe formed in the presence of a cationic surfactant such as benzalkoniumchloride, and then coated with an electrostatically bound hyaluronanlayer (Barbault-Foucher et al., 2002).

Several research groups have worked extensively on the formation ofcoatings that are formed by laying down alternatingelectrostatically-bound layers of hyaluronan and a cationic polymer. Thecoating is sometimes called a polyelectrolyte multilayer. The techniqueis frequently referred to as layer-by-layer assembly. The layers are notperfectly smooth, as the polymers have a tendency to form islands ofadsorbed material, and thus there can be extensive interpenetration ofthe anionic and cationic polymer layers. The coatings can be used tocarry bioactive agents (see below).

One research group has extensively investigated polyelectrolytemultilayers composed of hyaluronan and either polylysine or chitosan,usually deposited directly on glass or quartz substrates (Picart et al.,2001, 2002, 2005; Richert et al., 2004a, 2004b, 2004c, 2006; Collin etal., 2004; Zhang et al., 2005; Etienne et al., 2005; Schneider et al.,2006, 2007a, 2007b; Francius et al., 2006; Tezcaner et al., 2006). Usinga robotic coating device, the assemblies could be built with many (ca.20-100) layers. In some studies, the coatings were crosslinked afterdeposition. The stiffness parameters of the coatings were investigatedby nanoindentation of a colloidal probe tip in an atomic forcemicroscope, or by piezo-rheometer. It was observed that crosslinkingincreased stiffness and simultaneously increased cell adhesion. Thecrosslinked films were also resistant to enzymatic degradation. Thecrosslinked films were proposed to be useful in delivery of drugs suchas paclitaxel or diclofenac (see below). Most recently, assemblies ofhyaluronan with collagen protein, and hyaluronan with an aminatedderivative of hyaluronan were prepared and characterized.

Another research group has extensively studied polyelectrolytemultilayers formed with hyaluronan and chitosan (Thierry et al., 2003a,2003b, 2004, 2005; Kujawa et al., 2005, 2007). The coatings wereimmobilized on several different substrates, including polyethyleneimineon metal; polyethyleneimine on a carboxyalkylthiol-derivatized gold onsilica; quartz, and artery walls.

Additional groups have provided other very interesting and creativestudies of polyelectrolyte multilayers containing hyaluronan. Liu et al.(2006) prepared a hyaluronan-chitosan multilayer film for use in coatingpoly(ethylene terephthalate) in a microfluidic device. Veerabadran etal. (2007) built a hyaluronan-polylysine multilayer coating that wasable to encapsulate and protect stem cells. Lee at al. (2007b) devised aspherical microshell composed of a crosslinked hyaluronan-polylysinemultilayer, formed initially around a disulfide-crosslinked hyaluronanhydrogel microsphere that was liquified by reduction and allowed todiffuse out. The redox properties of polyelectrolyte multilayerscomposed of hyaluronan and the globular protein myoglobin have beenstudied as models for novel coatings for biosensors, bioreactors, andother biomedical devices (Liu and Hu, 2006; Lu and Hu, 2007).

Hyaluronan Attached to Supported Lipid Bilayers or Liposomes

Supported lipid bilayers can be used to immobilize hyaluronan. Senguptaet al. (2003) used a supported bilayer, deposited on glass, and formedwith a small fraction of lipid containing a nickel-chelating head group.Using histidine-tagged p32 protein that binds hyaluronan, thepolysaccharide was then bound noncovalently to the surface. Benz et al.(2004) used a lipid bilayer on mica to attach hyaluronan in severalways. A lipid carrying a biotin group allowed a layer of streptavidin tobe bound to the bilayer, and then biotin-labeled hyaluronan could benoncovalently bound to the surface. They also bound hyaluronancovalently to an amine-bearing lipid, using carbodiimide activation ofhyaluronan carboxyl groups. The bound hyaluronan layer could besubsequently crosslinked to form a stable coating. Richter et al. (2007)used the biotin-streptavidin-biotin technique to attach hyaluronan to alipid bilayer, but using hyaluronan end-labeled with biotin gave abetter result than the approach of Benz et al. (2004).

Margalit and coworkers pioneered the use of liposomes with boundhyaluronan. Attachment of hyaluronan via carbodiimide activation ofcarboxyl groups and reaction with amine-bearing lipids resulted instable hyaluronan-coated lipid vesicles (U.S. Pat. No. 5,401,511;Yerushalmi et al., 1994; Yerushalmi and Margalit, 1998; Peer andMargalit, 2000). The interior of the lipid vesicles could be loaded withgrowth factors for use in wound healing, or any of a number of drugs.The hyaluronan coat provided adhesion to certain types of cellsexpressing CD44 receptors, for extended residence time at the woundsite. The hyaluronan coat also provided protection of the liposomeduring lyophilization and reconstitution procedures that allow long termstorage of liposome-based therapeutics (Peer et al., 2003). Szoka andcoworkers (Eliaz and Szoka, 2001; Eliaz et al., 2004a, 2004b) producedliposomes with hyaluronan oligosaccharides bound to amine-bearing lipidsvia reductive amination. These liposomes could carry thechemotherapeutic agent doxorubicin, and target it to tumor cellsoverexpressing the CD44 receptor. The hyaluronan-coated liposomesprovided higher potency in tumor cell cytotoxicity, and lower toxicityto other cell types. Peer and Margalit (2004a, 2004b) furtherestablished the utility of high molecular weight hyaluronan as atargeting agent for liposomes carrying anti-tumor agents (doxorubicin,mitomycin C). Another use of hyaluronan-coated liposomes, proposed byMargalit and coworkers (Fischer et al., 2005), was as a carrier of anenzyme to protect against nerve toxin organophosphates. It should benoted that the hyaluronan coating in all of these liposome studies wasnot involved in binding or sequestering the bioactive agents, which wereencapsulated within the liposomes.

Surface-Immobilized Hyaluronan as a Carrier of Bioactive Agents

Layer-by-layer assemblies of hyaluronan and chitosan or hyaluronan andpolylysine have been suggested as carriers of bioactive agents such asarginine (Thierry et al., 2003a), sodium nitroprusside (Thierry et al.,2003b), paclitaxel (Schneider et al., 2007b) and sodium diclofenac(Schneider et al., 2007b). The enzyme trypsin, when immobilized on achitosan layer of a hyaluronan-chitosan multilayer film, was more activein protein digestion than free trypsin (Liu et al., 2006). Basicfibroblast growth factor (bFGF), adsorbed onto a polylysine layer of ahyaluronan-polylysine film, was more effective than free bFGF in aidingadhesion and maintaining differentiation of photoreceptor cells(Tezcaner et al., 2006). Covalent attachment of gelatin to ahyaluronan-chitosan film was used to aid fibroblast adhesion (Croll etal., 2006).

Chemically modified hyaluronan can also be incorporated into a surfacecoating. DTPA-modified hyaluronan in a coating has been suggested as acarrier of radionuclides to inhibit cell proliferation on stents(Thierry et al., 2004). Hyaluronan can be derivatized with the RGDpeptide that mediates cell adhesion, to facilitate integration of animplanted material with surrounding tissue, esp. bone (Pitt et al.,2003). Hyaluronan chemically derivatized with the drug paclitaxel wasused with chitosan to form a multilayer (Thierry et al., 2005). Sulfatedhyaluronan, with nearly 90% of the hydroxyl groups sulfated, has alsobeen extensively studied in attachment to surfaces. The sulfatedhyaluronan is so significantly modified that its properties are notsimilar to hyaluronan, but it has excellent anticoagulant activity. Ithas a variable affinity for cell adhesion, generally being more adhesivethan hyaluronan. In complexation with Cu+2 ions, it is angiogenic.Barbucci has published a number of reports concerning sulfatedhyaluronan on surfaces. (Chen et al., 1997; Magnani et al., 2000, 2004;Barbucci et al., 2000c, 2002b, 2002c, 2003b, 2005c, 2005d; Hamilton etal., 2005; Chiumiento et al., 2007)

Hyaluronan attached to silica has been reported to have altered proteinor cell surface interactions relative to free hyaluronan. The alteredinteractions can be due to the chemical changes in the polymer caused bythe procedures used to attach hyaluronan to a surface (e.g., effectiveloss of carboxyl groups). An example is the binding with apparentconformation change of the protein fibronectin on a surface containingphotoimmobilized hyaluronan, where the hyaluronan has lost carboxylfunction and has an extreme degree of attachment frequency (Barbucci etal., 2005c). Similarly, fibrinogen adsorbed onto a photoimmobilizedhyaluronan surface cannot bind platelets, but fibrinogen can do so ifindependently covalently attached to the surface (Chiumiento et al.,2007). Serum proteins can adsorb to a surface having photoimmobilizedhyaluronan, and some bind strongly enough that a combination ofdetergent, urea and dithioerythritol is required to release them(Magnani et al., 2004).

Citation of any document herein is not intended as an admission thatsuch document is pertinent prior art, or considered material to thepatentability of any claim of the present application. Any statement asto content or a date of any document is based on the informationavailable to applicant at the time of filing and does not constitute anadmission as to the correctness of such a statement.

SUMMARY OF THE INVENTION

The present invention is directed to a biocompatible material in theform of a solid, a water insoluble cross-linked gel (polymer) or aliposome, which contains a stable complex of TNF-stimulated gene 6protein (hereinafter referred to as “TSG-6”) and hyaluronan (HA). Thepresent invention includes a stable soluble complex of TSG-6 and HAreleased from the biocompatible material.

The present invention also represents an improvement over existinghyaluronan biocompatible products that are in solid, gel or liposomeform as it combines the anti-inflammatory properties of the TSG-6-HAcomplex with the anti-adhesive properties of the existing HAbiocompatible products.

The present invention further provides an improved method for using aHA-containing biocompatible material to treat in a patient in needthereof a disease, disorder or condition for which the biocompatiblematerial is effective, where the improvement is that HA is stablycomplexed with TSG-6.

A still further aspect of the present invention is directed to a methodfor locally inhibiting inflammation by locally introducing thebiocompatible material of the present invention into a patient in needthereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1D are graphs showing TSG-6-dependent binding of IαI HCs toCov-HA. FIG. 1A: 2 nM TSG-6 or 2 nM purified IαI were incubated alone ortogether for 2 hours at 37° C. in Cov-HA or Cov-NH. FIG. 1B: Increasingconcentrations of TSG-6 protein were incubated with human plasma diluted1:1000 in TTBS for 2 hours at 37° C. in Cov-HA. FIG. 1C: 50 nM TSG-6 wasincubated with various dilutions of human plasma in TTBS for 2 hours at37° C. in Cov-HA or Cov-NH. FIG. 1D: Human plasma, diluted 1:10 to1:1000, was incubated in the presence or absence of 5 nM TSG-6 for 2 hat 37° C. Each data point represents the mean of 6 wells±SE.

FIGS. 2A and 2B are graphs showing the stability of the bond between HCsand HA. FIG. 2A: 50 nM TSG-6 and human plasma diluted 1:1000 wasincubated for 2 hours at 37° C. in Cov-HA. Selected wells were thentreated with either 6 M guanidine HCL, 6 M guanidine HCl containing 8%LSB, or with 2×SDS-PAGE sample buffer for 15 min. FIG. 2B: Selectedwells were then treated with either 6 M guanidine HCl containing 8% LSB(15 min at ambient temperature), 50 mM NaOH (1 h at ambienttemperature), or 10 u/ml S. hyalurolyticus HAse (1 h at 37° C. Each datapoint represents the mean of 6 wells±SE.

FIGS. 3A and 3B are graphs showing simultaneous and sequential bindingof TSG-6 and HCs to HA. FIG. 3A: 5 nM TSG-6 and human plasma diluted1:1000 in PBS were incubated together in Cov-HA for 2 hours at 37° C.FIG. 3B: 5 nM TSG-6 in PBS was incubated in Cov-HA for 2 hours at 37° C.After washing with TTBS, human plasma diluted 1:1000 in PBS was added tothe same wells and incubated for 2 hours at 37° C. Both bound TSG-6 andbound HCs were determined. Each data point represents the mean of 6wells±SE.

FIGS. 4A and 4B are graphs showing the effect of EDTA on the HCtransfer. FIG. 4A: 2 nM TSG-6 and 2 nM purified IαI were co-incubated inthe absence or presence of 10 mM EDTA. FIG. 4B: 10 nM of TSG-6 in PBSwas incubated in the absence or presence of 10 mM EDTA. After washingwith TTBS, human plasma diluted 1:1000 in PBS was incubated in the samewells in the absence or presence of 10 mM EDTA. Each data pointrepresents the mean of 6 wells±SE.

FIGS. 5A and 5B are graphs showing the effect of the ionic strength onthe HC transfer to Cov-HA. FIG. 5A: TTBS, or 10 nM TSG-6 in TTBS wasincubated in Cov-HA for 2 h at 37αC. After washing with TTBS, eitherTTBS or human plasma diluted 1:1000 in TTBS was incubated in the samewells for 2 h at 37° C. Alternatively, 10 nM TSG-6 and plasma diluted1:1000 in TTBS were co-incubated for 2 h at 37° C. (TSG-6 +plasma). FIG.5B: PBS, or nM TSG-6 in PBS was incubated in Cov-HA for 2 h at 37° C.After washing with TTBS, human plasma diluted 1:1000 in either PBS, 20mM Tris pH 7.5, 150 mM NaCl, or 20 mM Tris pH 7.5, 500 mM NaCl, or 20 mMTris pH 7.5, 150 mM NaCl, 0.1% Tween-20, or 20 mM Tris pH 7.5, 500 mMNaCl, 0.1% Tween-20, was incubated in the same wells for 2 h at 37° C.Each data point represents the mean of 6 wells±SE.

FIG. 6 is a gel showing the transfer of HCs by HA-TSG-6 complexes. 100nM TSG-6 was incubated with 100 μl HA-Sepharose for 2 h at 37° C. Afterwashing with TTBS, the HA-Sepharose was incubated with human plasmadiluted 1:600 in either PBS or TTBS. Controls were incubated either withTTBS, TSG-6, or plasma only. All samples were treated with 10 u/ml HAsefrom Streptococcus hyalurolyticus. Released material was analyzed byimmunoblotting using either rabbit anti-TSG-6 or rabbit anti-HC, asindicated.

FIG. 7 is a gel showing the transfer of HCs by HA-TSG-6 complexes to adifferent HA strand. 100 nM TSG-6 was incubated with 100 μl HA-Sepharosefor 2 h at 37° C. After washing with TTBS, the HA-Sepharose wasincubated with human plasma diluted 1:600 and 100 μg/ml Select HA(molecular weight 30 kDa) in either PBS or TTBS for 2 h at 37° C.Controls were incubated either with TTBS, TSG-6 without plasma, orplasma without TSC-6 with Select HA. Supernatants containing Select HAbut not the immobilized HA were analyzed by immunoblotting using eitherrabbit anti-HC or HABP-bio.

FIGS. 8A-8D are gels showing that HC transfer in solution results information of HA-HC complexes, depletion of IαI and TSG-6-HC complexes,and generation of free bikunin. 20 nM TSG-6, human plasma diluted 1:600,and 100 μg/ml Select HA (30 kDa) were co-incubate for 2 h at 37° C.Controls for TSG-6 alone, plasma only, HA alone, TSG-6 plus plasma,TSG-6 and HA, and plasma and HA were also included. The reactionproducts were analyzed by immunoblotting using anti-HC (FIG. 8A),HABP-bio (FIG. 8B), anti-TSG-6 (FIG. 8C) or anti-bikunin (FIG. 8D).

FIG. 9 is a gel showing the formation of a stable (guanidine-resistant)bond between TSG-6 and HA Sponge B gel. 30 nM of TSG-6 in either TTBS(20 mM Tris pH 7.5, 500 mM NaCl, 0.1% Tween-20) (lanes 1, 2) or PBScontaining 5 mM MgCl₂ (lanes 3, 4), were incubated with 50 μl of HASponge B gel in a total volume of 200 μl at 37° C. for 2 h to form HASponge B-TSG-6 complexes. Two of the gels (lanes 2, 4) were then treatedwith 6 M guanidine HCl containing 8% lauryl sulfobetain for 15 min atambient temperature. This treatment is known to dissociate most proteinsnot bound covalently to hyaluronan. After extensive washing with TTBSand centrifugation in a Spin-X tube to remove all supernatant, the gelwas re-suspended in the Spin-X tube in 50 μl of 10 u/ml of Streptomyceshyaluronan lyase in PBS and incubated for 2 h at 37° C. Aftercentrifugation at 20,000 g for 3 min, the filtrate was collected foranalysis by immunoblotting using a rabbit anti-TSG-6 antibody.

FIG. 10 is a gel showing HC transfer from IαI to HA in solution bypre-formed HA Sponge B-TSG-6 complexes. 30 nM TSG-6 in TTBS (20 mM TrispH 7.5, 500 mM NaCl, 0.1% Tween-20) was incubated with 50 μl of HASponge B (gel sediment) in a total volume of 100 μl (adjusted with TTBS)at 37° C. for 2 h to form HA Sponge B-TSG-6 complexes (lanes 1, 2).Controls did not contain TSG-6 (lanes 3, 4). After extensive washingwith TTBS, the supernatants were carefully and completely removed.Thereafter, 200 μl of 100 μg/ml of SelectHA™ 30 kDa in PBS containing 5mM MgCl₂ and human plasma at a final dilution of 1:500 was added to thegel sediment and incubated 37° C. for 2 h to transfer HCs to the HA(lanes 1, 3). Alternatively, diluted plasma was added without HA as acontrol (lanes 2, 4). Thereafter, the supernatants were collected andanalyzed by immunoblotting using an anti-HC antibody for the presence ofHCs and HC-containing complexes. Note the consumption of IαI in thepresence of TSG-6 (lanes 1, 2). The HC-specific antibody recognizes aweak band of similar size as HA-HC in the absence of either HA (lane 2),TSG-6 (lane 3), or both (lane 4), which could be bikunin-HC, a commondegradation product of IαI. Lane 5 shows human plasma diluted 1:500.

FIG. 11 is a gel showing HC transfer from IαI to HA in solution bypre-formed HA Sponge B-TSG-6 complexes. The same supernatants as in FIG.10 were re-analyzed by immunblotting using the HA-specific probe HABP.Note that the HABP probe does not detect the weak band visible in FIG.10 in controls missing either TSG-6 or HA.

FIG. 12 is a gel showing formation of a stable bond between TSG-6 andHylan-B HA gel. 30 nM TSG-6 in TTBS (20 mM Tris pH 7.5, 500 mM NaCl,0.1% Tween-20) was incubated with 50 μl of Hylan-B gel in a total volumeof 100 μl at 37° C. for 2 h to form Hylan-B-TSG-6 complexes. The gel oflane 2 was then treated with 6 M guanidine HCl containing 8% laurylsulfobetain for 30 min at ambient temperature and washed extensivelywith TTBS. After centrifugation in a Spin-X tube to remove allsupernatant, the gel was re-suspended in the Spin-X tube in 50 μl of 10u/ml of Streptomyces hyaluronan lyase in PBS for 2 h at 37° C.Thereafter, after centrifugation at 20,000 g for 3 min, the filtrate wascollected and analyzed by immunoblotting using a rabbit anti-TSG-6antibody. Lane 3 contains recombinant TSG-6 as a control.

FIG. 13 is a gel showing HC transfer from IαI to HA in solution bypre-formed Hylan-B-TSG-6 complexes. 30 nM TSG-6 in TTBS (20 mM Tris pH7.5, 500 mM NaCl, 0.1% Tween-20) (lane 1), TBS (20 mM Tris pH 7.5, 500mM NaCl)(lane 2), PBS 5 mM MgCl₂ (lane 3), or PBS containing 5 mM MgCl₂and 0.1% Tween-20 (lane 4) was incubated with 50 μl of Hylan-B (gelsediment) in a total volume 100 μl at 37° C. for 2 h to formHylan-B-TSG-6 complexes. After extensive washing with TTBS, thesupernatants were carefully and completely removed. Thereafter, 200 μlof 100 μg/ml of SelectHA™ 30 kDa in PBS 5 mM MgCl₂ containing humanplasma at a final dilution of 1:500 was added to the gel sediment andincubated 37° C. for 2 h to transfer HCs to the HA. Thereafter, thesupernatants were collected and analyzed by immunoblotting using ananti-HC antibody for the presence of HCs and HC-containing complexes.Lane 5 shows human plasma diluted 1:500. Note the absence of the HA-HCcomplex in the plasma control (lane 5).

FIG. 14 is a gel showing HC transfer from IαI to HA in solution bypre-formed Hylan-B-TSG-6 complexes. The same supernatants as in FIG. 13were re-analyzed by immunblotting using the HA-specific probe HABP. Notethe absence of the HA-HC complex in the plasma control (lane 5).

FIG. 15 is a graph showing the stability of the bond between TSG-6 andCov-HA formed at 4° C. 10 nM purified recombinant TSG-6 in TTBS (20 mMTris pH 7.5, 500 mM NaCl, 0.1% Tween-20) was incubated for 16 hours at4° C. in Cov-HA or Cov-NH (as a control), as indicated. TTBS was usedinstead of TSG-6 as a control (lanes 1, 4). Selected wells (lanes 3, 6)were then treated with 6 M guanidine HCl containing 8% laurylsulfobetain at ambient temperature for 15 min. Bound TSG-6 protein wasthen determined with a rabbit anti-TSG-6 antibody. Each data pointrepresents the mean of 6 wells±SE.

DETAILED DESCRIPTION OF THE INVENTION

Inter-α-inhibitor (IαI), TSG-6 and hyaluronan (HA) participate in aseries of complex interactions that are functionally important ininflammation and fertility. Here, the present inventors show in theExample hereinbelow that stable hyaluronan-TSG-6 complexes are able tomediate the subsequent transfer of inter-α-inhibitor heavy chains tosurface-bound hyaluronan as well as to free hyaluronan in solution,suggesting that these complexes can simultaneously interact with asecond hyaluronan chain. Using a quantitative binding assay tocharacterize heavy-chain transfer to hyaluronan by free TSG-6 or bypreformed hyaluronan-TSG-6 complexes, the present inventors demonstratedthat TSG-6 and heavy chains can bind to surface-bound hyaluronan eithersimultaneously or in a two-step reaction. Interestingly, heavy chaintransfer by preformed hyaluronan-TSG-6 complexes and by free TSG-6 arecharacterized by different ionic strength requirements. The presentinventors also provide direct evidence in the Example hereinbelow that,when sufficient hyaluronan is present, the interaction of limitedamounts of TSG-6 with inter-α-inhibitor results in the generation offree bikunin, a serine protease inhibitor known to haveanti-inflammatory and anti-metastatic activities. Simultaneously, thisreaction results in the decrease of inter-α-inhibitor and in thegeneration of covalent hyaluronan-heavy chain complexes. A decrease ofinter-α-inhibitor concentrations in plasma has been observed in sepsis,while the generation of covalent hyaluronan-heavy chain complexes isknown to occur in rheumatoid arthritis, two conditions associated withthe expression of TSG-6.

Based on the findings of the present inventors, the present invention isdirected to a biocompatible material which is in the form of a solid, across-linked gel or liposomes and contains a stable complex ofTNF-stimulated gene 6 (TSG-6) and hyaluronan (HA).

The term “biocompatible” means that the material is compatible oracceptable for administration or implantation into the body or is in aform that is pharmaceutically acceptable.

The term “hyaluronan” as used herein further encompasses salts and freeacids of hyaluronan as well as hyaluronan that has been cross-linked orchemically altered, yet retain its function. These modificationsinclude, but are not limited to, esterification, sulfation,polysulfation, and methylation. Hyaluronan salts include, but are notlimited to, sodium hyaluronate, potassium hyaluronate, magnesiumhyaluronate, and calcium hyaluronate.

The term “stable” used herein as it relates to a complex of TSG-6 and HAis defined by the resistance of the TSG-6-HA complex to treatment withdetergents, dissociating and reducing agents. Specifically, “stable”TSG-6-HA complexes are resistant to treatment with 6M guanidine HClcontaining 8% lauryl sulfobetain(3-(Dodecyldimethylammonio)propanesulfonate, Zwittergent®). Thistreatment is known to break most noncovalent bonds between protein andHA (Mason et al., 1982; Tsiganos et al., 1986) and has been used to testthe stability of covalent protein-HA complexes (Yoneda et al., 1990). ATSG-6-HA complex that is referred to as “stable” is also resistant toboiling in reducing SDS-PAGE sample buffer (0.25 M Tris pH 6.8, 2%sodium dodecylsulfate, 5% 2-mercaptoethanol, 10% glycerol).

The TSG-6-HA complex, when bound to a solid surface or contained withina water-insoluble cross-linked gel or contained on or within a liposomeis able to transfer the heavy chains of inter-α-inhibitor (IαI), aubiquitous plasma protein, to surface-bound HA or free hyaluronan (insolution). When used in the biocompatible material of the presentinvention, TSG-6 protein's biological activities can be applied andmaintained locally at a site in the patient, either on the surface of anin-dwelling/implanted device or associated with a biocompatiblematerial, preferably a biodegradable biocompatible material.

Because the medical applications of soluble TSG-6 are limited by itsshort residence time in tissue as a consequence of its elimination withtissue fluid or its local metabolism, the present invention extends thetherapeutic utility of TSG-6 by prolonging its ability to locally modifyhyaluronan through transfer of IαI heavy chains, thereby focusing theeffect of TSG-6 in a defined temporal and spatial manner. Theinteraction of TSG-6 with IαI at the local site in a patient where thebiocompatible material is introduced, particularly in the presence ofHA, results in the local release of bikunin, a serine protease inhibitorwith anti-inflammatory activities and properties.

When the biocompatible material is present on the surface of a solidmedical device that is implantable or in-dwelling (e.g., stents,artificial joints, etc.) in a patient or is transiently introduced intoa patient during the course of a medical procedure (e.g., catheters,guidewires, etc.), the complex of TSG-6 and HA preferably forms acoating on such a solid medical device. In addition to coating such asolid medical device with the biocompatible (e.g., nano- andmicroparticles disclosed in WO 03/015755 and US2004/0241248, etc.)material in the form of a solid, a cross-linked gel or a liposome, thepresent invention also encompasses a biocoinpatible material whichinitially starts out as a solid dry powder of cross-linked HA or ofcross-linked mixed polymer of HA and at least one other polymer (i.e.,by itself as a solid dry powder or coating the surface of a solidimplantable medical device), which when hydrated with a solutioncontaining TSG-6, forms a cross-linked HA or cross-linked HA-containinggel in which the TSC-6-HA complex is a stable TSG-6-HA complex.

Also encompassed by the present invention is a biocompatible material inwhich the stable complex of TSG-6 and HA is capable of being releasedfrom the material in soluble form. This soluble form of the complex ofTSG-6 and HA is stable because it was originally formed on a solid, awater insoluble cross-linked gel or a water insoluble liposome, incontrast to complexes of TSG-6 and HA formed in solution.

The stable TSG-6-HA complex may also be used in the presentbiocompatible material as an injectable gel, wound dressing, nano- ormicroparticles or liposomes administered by surface application,injection (i.e., parenteral, intra-articular, etc) or implantation.There are many existing hyaluronan-based biocompatible materials thatare well-known in the art, such as the representative HA-containingmaterials disclosed in the above “Description of the Related Art”section, but these materials have limited anti-inflammatory activity. Bycoupling TSG-6 to such material in the form of a stable complex of TSG-6and HA, while maintaining the ability of TSG-6 to interact with IαI andtransfer the heavy chains of IαI to surface bound HA and to free HA insolution, biocompatible materials are generated that combineanti-adhesive and anti-inflammatory properties. Thus, the addition ofTSG-6 in a complex with HA in existing HA-based biocompatible materialsis a distinct improvement to the art. Accordingly, the present inventionalso provides an improved method for using existing HA-basedbiocompatible material, in the form of a hyaluronan attached to a solidor a liposome, or cross-linked in a cross-linked HA or HA-containinggel, to treat a disease, disorder or condition of which thebiocompatible material is effective. The improvement lies in the featureof HA in the existing biocompatible material being stably complexed withTSG-6.

The biocompatible material of the present invention is suitable for useto inhibit or treat various inflammatory pathologies, including but notlimited to intra-articular treatment of arthritic disease, inhibitingadhesion formation between internal wound surfaces after surgery,minimizing pathological changes between tissue surfaces and in-dwellingdevices, such as catheters, stents, etc., and providing ananti-inflammatory effect in combination with the wound-healing promotingeffects of HA.

The present invention further provides a method for locally inhibitinginflammation (at a local site) in a patient. This method involvesintroducing the biocompatible material locally into a patient in needthereof, i.e., by implanting or locally administering (i.e., injectingnano- or microparticles, cross-linked HA-containing gels or liposomes)to a local site in the patient.

The patient is preferably a human patient but may include other mammalssuch as dogs, cats, and horses. It is intended and preferred that theTSG-6 protein is native to the mammal (naturally occurring in themammalian species) which is to be treated with the TSG-6-HAcomplex-containing biocompatible material. Besides the human TSG-6sequence (SEQ ID NO:1) and allelic variants that have 99% nucleotidesequence identity (GenBank accession nos. AJ421518.1 and AJ419936.1) toSEQ ID NO:1, the TSG-6 sequence has been characterized in dog (SEQ IDNO:2; GenBank accession no. XM533354.2), horse (SEQ ID NO:3; GenBankaccession no. NM 001081906.1), orangutan (GenBank accession no.AC188102.1), mouse (GenBank XM001473344.1), rat (GenBank accession no.AF159103.1) and opossum (GenBank accession no. XM001365235.1) among anumber of others. TSG-6 protein from different mammalian species havehigh sequence homology/identity with each other (i.e., from 82% sequenceidentity at the nucleotide level between human and rat to 90% with humanand horse; and greater than 90% amino acid sequence identity betweenhuman TSG-6 and mouse, rabbit and rat TSG-6). This is not surprisingsince the activity of TSG-6 protein does not appear to bespecies-specific but is able to exert its activity across species.Consequently, while the TSG-6 is preferably native to the mammalianspecies which is to be treated by the biocompatible material containinga stable complex of TSG-6 and HA, it may be a non-native TSG-6 proteinfrom a different mammalian species or it may suitably be a variant ofthe native TSG-6 in which one or more, preferably no more than five,amino acid residues are substituted by residues that appear in TSG-6from other species at nonconserved residue positions.

Having now generally described the invention, the same will be morereadily understood through reference to the following examples which areprovided by way of illustration and are not intended to be limiting ofthe present invention.

Example 1

The goal of the study in this Example was to evaluate the role of freeTSG-6 and of surface-bound HA-TSG-6 complexes in the transfer of HCsfrom IαI in plasma to HA, using a quantitative assay system. Thesimultaneous binding of TSG-6 and HCs to surface-bound HA and thetransfer of HCs to surface-bound or free HA in a two-step reaction bypre-formed HA-TSG-6 complexes were investigated. Distinct sets ofproducts were found to be formed after binding of TSG-6 and HC transferto HA in solution or to solid-phase HA. The scale of HC transfer fromIαI in plasma to HA in the presence of added TSG-6 suggests thatTSG-6-mediated HC transfer is the major mechanism for the generation ofHA-HC complexes and, simultaneously, may significantly contribute to thedecrease of IαI in plasma and to the generation of free bikunin, aserine protease inhibitor with anti-inflammatory properties.

The abbreviations used herein are: Cov-HA, Covalink-HA; Cov-NH,Covalink-NH; EDC, N-ethyl-N′-(3-dimethylaminopropyl) carbodiimide; FES,fetal bovine serum; GAG, glycosaminoglycan; HA, hyaluronan; HABP-bio,biotinylated HA binding protein; IαI, inter-α-inhibitor; LSB, laurylsulfobetain; SE, standard error; pNPP, p-nitrophenyl phosphate;sulfo-NHS, N-hydroxysulfosuccinimide; TBS, Tris-buffered saline; TSG-6,TNF-stimulated gene 6 protein; TTBS, TBS containing 0.1% TWEEN-20.

Materials and Methods

Reagents. Covalink-NH plates were purchased from Nunc, sulfo-NHS fromPierce, and EDC was purchased from Sigma. HA from rooster comb waspurchased from Sigma and bacterial HA was obtained from LifecoreBiomedical, both of which were used for coupling to Cov-NH. Equivalentresults were obtained with Cov-HA prepared with rooster comb HA andbacterial HA. EAH-Sepharose was purchased from GE Healthcare,Piscataway, N.J. Hyaluronidase from Streptomyces hyalurolyticus andbiotinylated hyaluronan binding protein (HABP-bio) were purchased fromAssociates of Cape Cod, Falmouth, Mass. Select HA™ 30 kDa was purchasedfrom Hyalose L.L.C. (Oklahoma City, Okla.). Human plasma was obtainedfrom the blood bank of the NYU Medical Center. Rabbit anti-IαI was fromDako and is HC specific, i.e., it recognizes free HCs but it does notrecognize bikunin (data not shown). The rabbit anti-TSG-6 antibody wasraised against native recombinant TSG-6 and has been described earlier(Mindrescu et al., 2005). The rabbit anti-bikunin antibody was generatedand provided by Jan Enghild and Christian Sanggaard, University ofAarhus, Denmark.

Biotinylated goat anti-rabbit Ig was from Dako (Glostrup, Denmark) andstreptavidin-alkaline phosphatase conjugate was from Invitrogen(Carlsbad, Calif.). The alkaline phosphatase substrate was p-nitrophenylphosphate (Sigma, St. Louis, Mo.) for solution assays and BCIP/NBT fromBio-Rad for immunoblots. PDVF membrane for immunoblotting (Immobilon P)was from Millipore (Billerica, Mass.).

TSG-6 protein. TSG-6 protein was expressed in BTI-TN-5B1-4 insect cellsafter infection with recombinant nuclear polyhedrosis virus(baculovirus) and purified as described (Wisniewski et al., 1994 and2005).

Purified IαI. IαI was purified from human plasma as described previously(Wisniewski et al., 1996).

Coupling of HA to Covalink-NH plates and EAH-Sepharose.

HA was coupled to Covalink-NH plates as described (Wisniewski et al.,2005; and Frost et al., 1997). In brief, HA solution containingsulfo-NHS was added to the wells of Cov-NH plates.

After addition of EDC, the plates were incubated for 2 h at roomtemperature and overnight at 4° C. Thereafter, the plates were washedextensively with 2 M NaCl and blocked with 0.2% casein in TTBS.

Coupling of HA to EAH-Sepharose was carried out similarly to thecoupling of HA to Cov-NH. HA at 0.55 mg/ml in a 22.2% (v/v) suspensionof EAH-Sepharose was incubated with 0.89 mM sulfo-NHS and 0.36 mM EDC inH₂O for 2 h at room temperature and overnight at 4° C. under constantmovement. Thereafter, the HA-sepharose was washed with an at least10-fold volume of 2 M NaCl.

TSG-6 binding assay and HC transfer assay using HA immobilized toCovalink. The assay for TSG-6 binding to HA was carried out as described(Wisniewski et al., 2005). To determine HC transfer, TSG-6 at theindicated concentration was mixed with human plasma at the indicateddilution, usually 1:1000, in TTBS (TTBS: 20 mM Tris pH 7.5, 500 mM NaCl,0.1% TWEEN-20) and co-incubated in wells of Cov-HA plates for 2 h at 37°C. (100 μl/well). After washing 3 times with 200 μl of TTBS, the wellswere incubated with a 1:2000 dilution (in TTBS) of a rabbit anti-IαIantiserum that is HC specific, i.e., it does not detect bikunin, for 1 hat 37° C., followed by incubation with biotinylated goat anti-rabbit Ig(1:1000 in TTBS, 1 h at 37° C.). After incubation with astreptavidin-alkaline phosphatase:conjugate (1:1000 in TTBS, 1 h at 37°C.) and with p-nitrophenyl phosphate (2 mg/ml in 50 mM Tris pH 9.5, 2 mMMgCl2, 1 h at 37° C.), the amount of dephosphorylated substrate wasdetermined by measuring the absorbance at 410 nm, using 800 nm as areference wave length.

HC transfer to HA-sepharose. 100 μl of HA-sepharose (sediment) wasincubated with 200 μl of 400 nM TSG-6 in TTBS for 2 h at 37° C. Afterextensive washing with TTBS (three times 400 μl) the HA-sepharose wasincubated with a 1:100 dilution of human plasma in PBS (2 h at 37° C.).After extensive washing, as above, the HA-sepharose was treated with 100μl of 10 u/ml Streptomyces hyaluronidase (in PBS, 2 h at 50° C.). 100 μlof 2×SDS-PAGE sample buffer was added to the HA-sepharose and, aftervortexing, the liquid phase was recovered by centrifugation in a Spin-Xcolumn (Corning Inc., Corning, N.Y.). The recovered filtrate wasanalyzed by immunoblotting for the presence of TSG-6, HCs, TSG-6-HCcomplexes etc. using HC— and TSG-6-specific antibodies. Controls weretreated either only with TSG-6, or only with plasma, or without TSG-6and plasma. In order to discern between HC transfer by free TSG-6 vs.HA-TSG-6 complexes, the incubation with plasma was also carried out inTTBS instead of PBS, for reasons more fully described under the Resultssection below.

HC transfer by solid-phase HA-TSG-6 complexes to HA in solution. TSG-6was bound to HA-sepharose as described above. 100 μl of HA-sepharose(sediment) was incubated with 200 μl of 100 nM TSG-6 in TTBS for 2 h at37° C. After extensive washing with TTBS (three times 400 μl) theHA-sepharose was incubated with 100 μl of a 1:600 dilution of humanplasma in PBS containing 100 μg/ml Select HA™ of 30 kDa (2 h at 37° C.).100 μl of 2×SDS-PAGE sample buffer was added to the HA-sepharose and,after vortexing, the liquid phase was recovered by centrifugation in aSpin-X tube (Costar). The recovered filtrate was analyzed byimmunoblotting for the presence of HA-HC complexes using HC-specificantibodies and a HA-specific HABP probe. Controls were treated eitheronly with TSG-6, or only with plasma, or without TSG-6 and plasma. Inorder to discern between HC transfer by free TSG-6 vs. HA-TSG-6complexes, the incubation with plasma was also carried out in TTBSinstead of PBS.

Formation of HA-HC complexes in solution. 20 nM TSG-6, 100 μg/ml SelectHA, and human plasma diluted 1:600 were co-incubated for 2 h at 37° C.in PBS and the reaction products were analyzed by immunoblotting for thepresence of TSG-6, IαI, HCs, TSG-6-HC complexes, HA-HC complexes, andfree bikunin using HC—, TSG-6-, or bikunin-specific antibodies or theHA-specific HABP probe. Controls contained either one or two of thethree components (TSG-6, plasma, HA).

Results

TSG-6 Mediates Transfer of HCs from IαI to Immobilized HA

IαI has been reported to be physically associated with HA in synovialfluids of patients with rheumatoid arthritis, but not in synovial fluidsof normal human subjects, and the formation of HA-HC complexes has beendescribed after co-incubation of HA with normal bovine or human serum(Huang et al., 1993; Becker et al., 1971; Hamerman et al., 1966; andSandson et al., 1965). On the other hand, TSG-6 forms stable complexeswith HCs of IαI and can transfer them to HA (Mukhopadhyay et al., 2004;Rugg et al., 2005; and Jessen et al., 2004). It is currently not clearif TSG-6 is essential for HC transfer to HA to occur or if there arealternative pathways independent of TSG-6. In order to investigate thisquestion, HA coupled covalently to the surface of Covalink-NH plates(Cov-HA) was used. Cov-HA was previously used to study the binding ofTSG-6 to HA (Wisniewski et al., 2005).

The transfer of HCs to Cov-HA was analyzed after incubation of IαI inCov-HA either in the absence or in the presence of recombinant TSG-6 inCov-HA, followed by stringent washing, and detection by a rabbit anti-HCantibody that reacts with IαI and HCs, but does not detect bikunin. Asshown in FIG. 1A, there was virtually no binding of purified human IαI,or its HCs, to immobilized HA in the absence of TSG-6. HC binding to HAwas readily detectable if purified TSG-6 is added to purified IαI. Thequantitative assay does not distinguish between bound HCs or completeIαI, and this issue is further addressed below.

In order to investigate whether the lack of HC transfer from purifiedIαI to Cov-HA is an artifact resulting from partial denaturation of thiscomplex protein during its purification, the transfer of HCs from IαI inplasma to immobilized HA was examined. FIG. 12 shows that the transferof HCs from IαI in diluted human plasma to Cov-HA is also completelydependent on the presence of added TSG-6 protein. As little as 16 μMTSG-6 is sufficient to mediate detectable transfer of HCs from IαI inhuman plasma to Cov-HA (FIG. 1B). The average concentration of IαI inhuman plasma is about 700 mg/l (Baek et al., 2003). The laboratory ofthe present inventors tested how the plasma concentration affects thebinding of IαI to HA (FIG. 1C). With respect to HC transfer to Cov-HA inthe presence of TSG-6, the IαI concentration in human plasma issaturating, and a 1:100 dilution of human plasma did not result in anydecrease of HC transfer. Even at a 1:4000 dilution of plasma thetransfer of HCs to HA was only decreased by about 50%, and HC transferwas still detectable at a plasma dilution of 1:16000. This means thatconcentrations of unpurified IαI of as little as 200 μM are sufficientfor detectable HC transfer to HA. Interestingly, some HC transfer toCov-HA could be detected in the absence of exogenous TSG-6 at highplasma concentrations (FIG. 1D). However, a plasma dilution of 1:1000completely abolished any detectable transfer, while TSG-6-dependent HCtransfer at this plasma dilution was not affected (FIG. 1D), making itunlikely that the IαI concentration is the factor limiting the HCtransfer in the absence of exogenous TSG-6.

Stability of the Bond between HCs and Immobilized HA

The present inventors reported earlier that TSG-6 forms a remarkablystable bond to immobilized HA in a strictly temperature-dependentfashion. Using the same assay system, IαI HCs found to be transferred toimmobilized HA in the presence of 50 nM TSG-6 are also almost completelyresistant to treatment with 6 M guanidine HCl, 6 M guanidine HClcontaining 8% LSB, or SDS-PAGE sample buffer containing2-mercaptoethanol (FIG. 2A). However, they were sensitive to treatmentwith hyaluronidase from Streptomyces hyalurolyticus and, in contrast toHA-TSG-6 complexes, they were also sensitive to treatment with dilutedalkali, in agreement with the presence of an ester bond between HA andHC in HA-HC complexes (Zhao et al., 1995) (FIG. 2B). This providesevidence that the HC transfer observed on Cov-HA yields productsindistinguishable from the ones observed with HA in solution.

Simultaneous vs. Sequential TSG-6 Binding and HC Transfer to Cov-HA

Because TSG-6 itself binds to Cov-HA under the conditions used toevaluate HC transfer to Cov-HA, as shown previously (Wisniewski et al.,2005), the present inventors investigated if both TSG-6 binding and HCtransfer to Cov-HA can occur simultaneously. After co-incubation ofTSG-6 and diluted plasma in Cov-HA, providing conditions forsimultaneous binding of TSG-6 and HC transfer, both TSG-6 and IαI HCscould be detected attached to the surface-bound HA (FIG. 3A).

Because TSG-6 binding to Cov-HA resulted in the formation of stablecomplexes (Wisniewski et al., 1994), the present inventors alsoinvestigated if preformed HA-TSG-6 complexes are able to mediate thetransfer of HCs from IαI to Cov-HA in a two-step reaction. FIG. 3B showsthat TSG-6, after binding to Cov-HA under conditions that result in theformation of stable HA-TSG-6 complexes, is able to mediate thesubsequent transfer of HCs to the Cov-HA substrate after all solubleTSG-6 has been removed by extensive washing. This Cov-HA binding assaycannot distinguish between HCs bound directly to HA, i.e., HA-HCcomplexes, and HCs bound to TSG-6, i.e., HA-TSG-6-HC complexes. Thisquestion will be addressed separately using a different experimentalapproach (see below).

Transfer of IαI HCs to Immobilized HA is Strictly Dependent on MetalIons

It was established earlier that the transfer of HCs to HA is dependenton the presence of divalent metal ions and could be prevented by theaddition of EDTA (Rugg et al., 2005; Jessen et al., 2004; and Odum etal., 2002). FIG. 4A confirms that the TSG-6 dependent transfer of HCs toCov-HA is completely prevented by the presence of 10 mM EDTA, atreatment that does not prevent the binding of TSG-6 to immobilized HA(Wisniewski et al., 2005). The role of metal ions on the individualsteps of the 2-step reaction described above, i.e., the transfer of HCsto Cov-HA by pre-formed Cov-HA-TSG-6 complexes, was also determined.While the presence of EDTA during the binding of TSG-6 to Cov-HA has amodest effect on the transfer of HCs in the following step, the presenceof EDTA during the second step, the interaction of pre-formed HA-TSG-6complexes with IαI, completely prevented any HC transfer (FIG. 4B). Thepartial inhibitory effect of EDTA during the binding of TSG-6 to Cov-HAon the subsequent transfer of HCs is in good agreement with a similareffect of EDTA on the binding of TSG-6 to Cov-HA itself (Wisniewski etal., 2005).

Differential Ionic Strength Requirements for the Transfer of HCs by FreeTSG-6 or Pre-Formed HA-TSG-6 Complexes

While the binding of TSG-6 to Cov-HA and the simultaneous transfer ofHCs can be carried out in TTBS, i.e., in the presence of Tris buffer,500 mM NaCl and 0.1% TWEEN-20, (FIGS. 1A-D, 5A), the sequential transferof HCs by pre-formed HA-TSG-6 complexes required PBS and was completelysuppressed in TTBS (FIG. 5A). In order to determine if the failure ofsequential HC transfer was the result of the difference in ionicstrength or the result of the presence of the non-ionic detergent,TWEEN-20, in TTBS, or the different ions in the two buffer systems, thesecond step of the sequential HC transfer, i.e., the transfer of HCs bypreformed HA-TSG-6 complexes, was carried out in either PBS, Tris bufferpH 7.5 containing 150 mM NaCl, Tris buffer pH 7.5 containing 500 mMNaCl, Tris buffer pH 7.5 containing 150 mM NaCl and 0.1% TWEEN-20, orTris buffer pH 7.5 containing 500 mM NaCl and 0.1% TWEEN-20 (TTBS). Ascan be seen in FIG. 5B, the second step of the sequential HC transfer iscompletely inhibited in the presence of 500 mM NaCl, but not by thepresence of TWEEN-20, or by the different buffers used. Thisdifferential ionic strength requirement for the simultaneous and thetwo-step, or sequential transfer of HCs can therefore be used todifferentiate between the two binding mechanisms, i.e., two-steptransfer of HCs by HA-TSG-6 complexes is completely inhibited in 500 mMNaCl.

HC Transfer by Pre-Formed HA-TSG-6 Complexes Bound to Sepharose Resultsin HA-HC Complexes

Pre-formed HA-TSG-6 complexes interact with IαI, resulting in thetransfer of HCs to the HA substrate.

Presumably, the first step of this transfer is the formation of aHA-TSG-6-HC complex, in analogy to the formation of TSG-6-HC complexesin the absence of HA. These HA-TSG-6-HC complexes may transfer HC in anadditional step to HA, resulting in HA-HC complexes as final products,in analogy to HA-HC complexes formed with HA free in solution.Alternatively, HA-TSG-6-HC complexes could be the final product. Thesealternatives raise an important question because they would result instructurally different modifications of surface-bound HA vs. HA free insolution.

In order to determine whether HC transfer by preformed HA-TSG-6complexes results in a final HA-HC complex, or alternatively in aHA-TSG-6-HC complex, TSG-6 bound to HA-sepharose under conditionsresulting in the formation of stable HA-TSG-6 complexes were employed(Wisniewski et al., 2005). After stringent washing to remove all freeTSG-6 protein, the HA-TSG-6 complexes were incubated with plasma, as asource of IαI, washed again, and then treated with hyaluronidase from S.hyalurolyticus to release HA fragments and attached proteins from thesepharose. The recovered products were then analyzed by immunoblottingfor the presence of either free HCs or TSG-6-HC complexes. In order toexclude the possibility that the HC transfer is due to the presence ofresidual free TSG-6, instead of HA-TSG-6 complexes, the incubation withdiluted plasma was carried out either in TTBS or in PBS, as describedabove. FIG. 6 demonstrates that hyaluronidase treatment releases TSG-6(left panel) and HCs (right panel), whereas no TSG-6-HC complexes couldbe detected. When the reaction between pre-formed HA-TSG-6 and plasmawas carried out in TTBS, no HCs were transferred to the HA-sepharose(right panel), and the hyaluronidase treatment releases only the boundTSG-6 (left panel). This suggests that preformed HA-TSG-6 complexes wereresponsible for the observed transfer reaction, and that all of the HCs“captured” from IαI were directly transferred to HA. The diffuse natureof the HC bands in FIG. 6 (right panel) may be a consequence of residualHA fragments remaining attached to the HCs after hyaluronidasedigestion. The finding that no TSG-6-HC complexes were released by thehyaluronidase treatment strongly suggests that HA-TSG-6-HC complexes arenot a final product of this reaction.

HC Transfer by Surface-Bound HA-TSG-6 Complexes to HA Chain in Solution

The experimental protocol to determine whether preformedsepharose-HA-TSG-6 complexes are able to transfer HCs from IαI to HAmolecules in solution, i.e., to a different HA chain than the onebinding TSG-6 on the solid surface, was modified. TSG-6 was incubatedwith HA-Sepharose in the first step of this protocol, as describedabove, to form stable sepharose-HA-TSG-6 complexes. In the second step,the HA-TSG-6 complexes were incubated with diluted plasma plus HA insolution (Select HA, 30 kDa), an HA preparation with a narrow molecularmass distribution. After the incubation, the liquid phase of thereaction mixture was analyzed by immunoblotting for the presence ofHA-HC complexes. In order to exclude the possibility that the HCtransfer is due to the presence of free TSG-6, instead of HA-TSG-6complexes, the incubation with diluted plasma and Select HA was carriedout either in TTBS or in PBS, as described above (FIGS. 5A and 5B). FIG.7 shows that HA-HC complexes with Select HA are indeed formed in PBS,but not in TTBS, demonstrating that the Sepharose-HA-TSG-6 complex isable to transfer HCs to HA molecules in solution, and suggesting thatHA-TSG-6 complexes are responsible for the HC transfer. These dataindicate that TSG-6 bound to the immobilized HA is able to transfer HCsto a different HA chain free in solution.

TSG-6-Mediated HC Transfer can Deplete IαI and Generate Free Bikunin

All the previous experiments were carried out using surface-bound HA asat least one of the reactants. When TSG-6 and plasma, as a source ofIαI, are co-incubated in the absence of HA, TSG-6-HC complexes are amajor species detected (FIGS. 8A and 8C). However, when Select HA isincluded in the reaction mixture, HA-HC complexes are the major speciesdetected (FIGS. 8A and 8B). HA-HC complexes are detected both by ananti-HC antibody (FIG. 8A) and by the HA-detecting HABP-bio probe (FIG.8B). The lack of detection of free HA by this probe is due to thefailure of free HA to blot to the PVDF membrane—it can be detected by anHABP-bio affinity probe after transfer to positively charged blottingmembranes (data not shown).

Notably, the presence of both TSG-6 and Select HA in the reactionmixture, resulted in significant depletion of the available IαI (FIG.8A) and the generation of free bikunin (FIG. 8D). When only TSG-6 wasadded to plasma, less bikunin was generated and more IαI remained,suggesting that the presence of HA as acceptor for HC transfercontributes to IαI depletion and the generation of free bikunin.

Interestingly, while the interaction of TSG-6 with immobilized HAresulted in the formation of stable HA-TSG-6 complexes (Wisniewski etal., 2005), there is no indication that the interaction of TSG-6 with HAin solution resulted in the generation of stable HA-TSG-6 complexes(FIG. 8C). Because the transfer of HCs to HA in solution was strictlyTSG-6-dependent, the interaction of TSG-6 or TSG-6-HC complexes with HAhas to be considered a prerequisite to the transfer of HCs to HA.However, this interaction did not, in contrast to the interaction ofTSG-6 with surface-bound HA, result in stable binding of TSG-6 to HA.

Discussion

Components of the plasma proteinase inhibitor IαI have been known formany years to associate tightly with HA in the synovial fluid ofpatients with rheumatoid arthritis. However, while the complex structureof IαI remained unresolved for over two decades, the composition of thecomplexes, and in particular the presence of the bikunin chain, was notaddressed in those early studies (Becker et al., 1971; and Sandson etal., 1965). Later, it became clear that HA in synovial fluid ofrheumatoid arthritis patients was associated with HCs only, and not withcomplete IαI (Huang et al., 1993). Interestingly, HA-HC complexes couldbe generated by co-incubation of HA with either normal human or bovineserum, leading to the suggestion that the HCs of IαI bind to HAspontaneously (Huang et al., 1993). However, the few reports thataddressed the interaction between purified IαI, or its HCs, and HAexperimentally, did not provide evidence for the formation of stableHA-HC complexes under physiological conditions, and the only directinteraction between HCs and HA was limited to conditions of low ionicstrength, and the stability of the resulting complexes was notinvestigated (Chen et al., 1994; and Jean et al., 2001). In contrast,the catalytic role of TSG-6 for the transfer of HCs to HA and to HAoligosaccharides and the formation of stable HA-HC complexes in solutionhas been convincingly demonstrated (Mukhopadhyay et al., 2004; Rugg etal., 2005; and Jessen et al., 2004).

The data presented in this Example show that no HC transfer to HA occurswith purified IαI, or with highly diluted plasma, in the absence ofTSG-6, but that added TSG-6 in picomolar concentrations catalyzes HCtransfer (FIGS. 1A and 1B). HC transfer in the presence of TSG-6 isdetectable with plasma diluted as much as 1:16,000, equivalent to an IαIconcentration of about 200 pM. In agreement with published data (Huanget al., 1993), it was found that some HC transfer to HA can take placein plasma in the absence of added TSG-6, although the amount oftransferred HCs is small compared to TSG-6-mediated transfer. Thepresent inventors cannot rule out that this modest HC transfer is theresult of trace amounts of TSG-6 in normal plasma that are below thedetection limit of currently available antibody-based assays.Significant generation of HA-HC complexes in vivo has been associatedwith rheumatoid arthritis (Becker et al., 1971; Sandson et al., 1965;and Kida et al., 1999). It is therefore significant that TSG-6 was foundin synovial fluid of patients with rheumatoid arthritis, osteoarthritis,Sjögren's syndrome, polyarthritic gout, and osteomyelitis (Wisniewski etal., 1993). In addition, immunoblots of these synovial fluids revealedstable complexes of TSG-6 with HCs of IαI (Wisniewski et al., 1994; andWisniewski et al., 1993). The presence of TSG-6 and of TSG-6-HCintermediates in synovial fluids of patients with various inflammatoryjoint conditions strongly supports a significant role for TSG-6 in thegeneration of HA-HC complexes.

The present inventors show in this Example that preformed surface-boundHA-TSG-6 complexes are, like TSG-6 in solution, able to interact withIαI and transfer HCs to HA (FIG. 32). This alternative pathway of HA-HCcomplex formation may become significant in instances when the localexpression of TSG-6 precedes the influx of IαI from the vascularcompartment. The present inventors could also demonstrate that the finalproduct of this alternative reaction is the same as after HC transfer byfree TSG-6, i.e., a HC directly cross-linked to HA (FIG. 6). This isconsistent with the structure of the HA-HC complexes identified insynovial fluid of patients with rheumatoid arthritis (Zhao et al.,1995).

While HC transfer mediated by TSG-6 in solution readily proceeds in thepresence of 500 mM NaCl, HC transfer by HA-TSG-6 complexes bound to asolid phase is completely suppressed (FIG. 5). Although this effect ofhigh ionic strength may not have a physiological parallel, it provides aconvenient experimental tool to differentiate between the single phaseand the two phase reaction and suggests differences in the mechanism ofthe HC transfer.

HA-HC complexes formed on the solid substrate were resistant totreatment with dissociating and reducing agents, but sensitive totreatment with mild alkali or HAse (FIGS. 2A and 2B). The alkalisensitivity is consistent with the presence of an ester bond linking HCand HA, in analogy to the bonds that have been determined in HA-HCcomplexes from rheumatoid synovial fluid, and the ester bonds linkingchondroitin sulfate and HCs in IαI (Enghild et al., 1991; and Zhao etal., 1995). The sensitivity of HA-HC complexes to alkali treatment is inmarked contrast to HA-TSG-6 complexes formed on the Covalink substrate,that are alkali resistant (Wisniewski et al., 2005).

The question of whether HA-TSG-6 complexes can transfer HCs to adifferent HA chain was also addressed. The data shown in FIG. 7 showthat TSG-6, bound to immobilized HA, was able to transfer HCs to HA insolution. This is mechanistically interesting because it suggests theinteraction of a putative intermediary HA-TSG-6-HC complex with a secondHA chain.

With respect to the fate of the HCs, transfer by TSG-6 to HA in solutionis very similar to transfer to solid-phase HA, e.g., TSG-6-HC complexesare formed as intermediates but, in the presence of sufficient HA, arealmost completely depleted in the final transfer of HCs to HA (FIGS. 8Aand 8C). However, a notable difference between HC transfer to HA insolution and to surface-bound HA is that there is no evidence for theformation of stable HA-TSG-6 complexes with HA in solution (FIGS. 8B and8C).

The present inventors have shown earlier that the formation of stablecomplexes between TSG-6 and surface-bound HA is the result of a two-stepreaction with different temperature requirements. At 4° C., TSG-6 bindsto Cov-HA but can be easily dissociated, whereas the Cov-HA-TSG-6complex formed at 37° C. is resistant to dissociative and reducingconditions (Wisniewski et al., 2005). Although this phenomenon isoutside the scope of this study, the data suggest that TSG-6 is able todifferentiate between HA in solution and surface-bound HA and formsstable complexes only with surface-bound HA. The mobility of HA intissues varies widely, from free HA in solution in synovial fluid and HAbound to cellular surfaces via HA receptors, forming a pericellularmatrix, to HA complexed with proteoglycans and tightly packed into acollagen network in cartilage. Nevertheless, it is currently not clearwhat the physiological equivalent of surface-bound HA is.

The transfer of HCs from IαI to HA by TSG-6 results in the formation offree bikunin (FIG. 8D). In the presence of TSG-6 and sufficient HA, IαIcan be almost completely depleted, and HA-HC complexes and free bikuninare the final products (FIGS. 8A, 8B and 8D). A decrease of IαI inplasma or serum has been observed in association with infectious diseaseand sepsis and the concentration of IαI in the serum of sepsis patientshas been correlated with the outcome of the disease (Baek et al., 2003;Balduyck et al., 2000; Lim et al., 2003; and Opal et al., 2007). Inaddition, administration of exogenous IαI reduced mortality andmaintained hemodynamic stability in experimental models of sepsis (Wu etal., 2004; and Yang et al., 2002). The decrease of IαI concentrations inblood associated with disease is usually considered to be the result ofproteolytic degradation by neutrophil elastase or similar enzymes(Balduyck et al., 1993 and 2000; and ZHirose et al., 1998). Data fromthe present inventors suggest that TSG-6 and HA can also efficiently“degrade” IαI, simultaneously generating HA-HC complexes and freebikunin. The present inventors have reported earlier the presence ofTSG-6 in sera of sepsis patients and in sera of volunteers treated withTNF-α suggesting that involvement of TSG-6 in the degradation of IαI isfeasible (Wisniewski et al., 1997).

The pathophysiological role of IαI “degradation”, in contrast to low IαIlevels, is not necessarily a detrimental one. While IαI degradation isassociated with bikunin generation, low IαI levels entail depletion of abikunin precursor. Bikunin, or urinary trypsin inhibitor, has beenassociated with many beneficial activities, prominently among themanti-inflammatory effects (Pugia et al., 2005). While the serineprotease inhibitory activity of bikunin may account for many of theseeffects, some effects of bikunin may be mediated by a bikunin-specificcellular receptor, which may not interact with the bikunin of IαI due tosteric interference from its covalently attached HCs (Pugia et al.,2005). The ability of IαI to improve hemodynamic stability in anexperimental model of sepsis is similar to effects attributed to bikunin(Molor-Erdene et al., 2005). Therefore, free bikunin may be the activeagent responsible for some of the effects attributed to IαI.

While the modifications of HA and the turnover of I□I caused by thepresence of TSG-6 protein are becoming increasingly clear, thephysiological activities of the newly generated HA-HC complexes andpotential differences between the activities of I□I and bikunin arestill not well understood. The elucidation of these activities willfinally contribute to the understanding of the mechanism of action ofTSG-6, which has been consistently associated with anti-inflammatory andchondroprotective effects in experimental models of acute inflammationand arthritis.

Example 2 Binding of Recombinant TSG-6 to Radiation CrosslinkedHyaluronan and Capacity of the Complex to Transfer Heavy Chains fromInter-α-inhibitor to Hyaluronan in Solution

The goal of this study was to demonstrate that, in addition tohyaluronan (HA) associated with a solid surface, as shown in Example 1,crosslinked HA in the form of a hydrated gel is also able to form stablecomplexes with TSG-6 protein and that these HA-TSG-6 complexes are ableto subsequently interact with the plasma protein inter-α-inhibitor (IαI)and to transfer heavy chains (HC) from IαI to water-soluble HA that isin contact with the crosslinked HA gel. In order to demonstrate thisability of TSG-6 to stably modify a cross-linked HA-based gel, acrosslinked HA gel prepared according to U.S. Pat. No. 6,610,810,hereafter referred to as “HA Sponge B”, was used.

Materials and Methods

Reagents. Hyaluronidase from Streptomyces hyalurolyticus andbiotinylated hyaluronan binding protein (HABP-bio) were purchased fromAssociates of Cape Cod. SelectHA™ 30 kDa was purchased from HyaloseL.L.C. Human plasma was obtained from the blood bank of the NYU MedicalCenter. Rabbit anti-human IαI was from Dako. Although this antibody wasraised against IαI, it did not detect bikunin in immunoblotting andELISA and is therefore referred to as HC-specific. The rabbit anti-TSG-6antibody was raised against native recombinant TSG-6 and has beendescribed (Mindrescu et al., 2005). Biotinylated goat anti-rabbit Ig wasfrom Dako and streptavidin-alkaline phosphatase conjugate was fromInvitrogen. The alkaline phosphatase substrate was BCIP/NBT from Bio-Radfor immunoblots. PDVF membrane for immunoblotting was from Millipore(Immobilon P). HA Sponge B gel was obtained from the Matrix BiologyInstitute (Edgewater, N.J.) as a hydrated gel suspended in dH₂O.

TSG-6 protein. TSG-6 protein was expressed in BTI-TN-5B1-4 insect cellsafter infection with recombinant nuclear polyhedrosis virus(baculovirus) and purified as described (Wisniewski et al., 1994 and2005).

Binding of TSG-6 to HA Sponge B gel. HA Sponge B gel was stored as ahydrated gel suspended in dH₂O. Before a binding experiment, the gel waswashed extensively and equilibrated with the buffer to be used in theexperiment, either TTBS (20 mM Tris pH 7.5, 500 mM NaCl, 0.1% Tween-20)or PBS containing 5 mM MgCl₂. The gel was then incubated with a definedconcentration of recombinant TSG-6 at 37° C. for 2 h under constantrotation to facilitate contact of TSG-6 with the gel particles. Finally,the gel was washed extensively with TTBS to remove any free TSG-6.

Transfer of HCs by HA gel-TSG-6 complexes. The washed HA Sponge B gelcontaining complexes with TSG-6 was incubated with diluted human plasmaas a source of IαI at a final dilution of 1:500 (i.e., ca. 6 nM IαI) inthe presence of SelectHA™ 30 kDa, the latter to evaluate whether theTSG-6-HA Sponge B complex was able to transfer HCs from IαI to theSelectHA™ 30 kDa in the aqueous phase. The incubation was carried out inPBS containing 5 mM MgCl₂. The supernatant containing the SelectHA™ 30kDa was then collected and analyzed by immunoblotting for the presenceof HA-HC complexes. Immunoblotting was carried out using 12%polyacrylamide gels and denaturing conditions (2% SDS, 5%2-mercapthethanol), and PVDF as blotting membrane.

Results

Formation of stable HA-TSG-6 complexes. After incubation of recombinantTSG-6 with the HA Sponge B gel for 2 h at 37° C. in either TTBS or inPBS containing 5 mM MgCl₂, the gel was washed extensively in TTBS, toremove all TSG-6 that was not tightly bound, and either left in TTBS ortreated with the denaturing agent 6M guanidine HCl containing 8% oflauryl sulfobetain (LSB). After degradation of the gels usingStreptomyces hyaluronan lyase, the degraded gel was analyzed byimmunoblotting for the presence of TSG-6. FIG. 9 shows that TSG-6protein was found associated with HA Sponge B gel after incubation andwashing in either TTBS (lane 1) or PBS containing 5 mM MgCl₂ (lane 3).Although treatment with 6M guanidine HCl containing 8% LSB resulted in adecrease of the amount of TSG-6 associated with the HA gel, TSG-6forming a guanidine-resistant, i.e., stable, bond could be detectedafter incubation of TSG-6 with HA Sponge B gel in either TTBS (lane 2)or PBS containing 5 mM MgCl₂ (lane 4).

HC transfer by pre-formed HA Sponge B-TSG-6 complexes. FIG. 10 shows thepresence of HA-HC complexes, the product of HC transfer from IαI to HAin solution, after the incubation of pre-formed TSG-6-HA Sponge Bcomplexes with SelectHA™ in the presence of diluted human plasma as asource of IαI (lane 1). A weak band of about the same size as the HA-HCcomplex is also visible in lane 5, which is a plasma control (plasmadiluted 1:500). It is possible that this lane represents a bikunin-HCcomplex, a common degradation product of IαI that has a very similarsize as the HA-HC complexes. In order to confirm the nature of the banddetected in lane 1 of FIG. 9 as HA-HC complex, the same material wasre-analyzed by immunoblotting using the HA-specific probe HABP insteadof the HC-specific antibody. FIG. 11 confirms the identity of the bandformed in lane 1 as HA-HC complex. The HA-specific HABP probe detected aband of the same size exclusively in lane 1, i.e., the complex wasformed exclusively after the presence of both TSG-6 in the firstincubation and both plasma and SelectHA™ in the second incubation, butnot in the absence of either HA (lane 2) or TSG-6 (lane 3), or both(lane 4).

Discussion

The data presented in FIG. 9 show that recombinant TSG-6 binds readilyto HA Sponge B gel and also, to a lesser degree, forms aguanidine-resistant bond with this gel. Treatment with 6 M guanidine HClcontaining 8% of lauryl sulfobetain has been shown to dissociate mostnon-covalent bonds between hyaluronan and associated proteins (Mason etal., 1982; Tsiganos et al., 1986; and Yoneda et al., 1990). It is alsoshown in this Example that TSG-6 bound to HA Sponge B gel in afirst-step binding reaction is able to transfer HCs from IαI toSelectHA™ in a subsequent second step (FIGS. 10 and 11).

Example 3 Binding of Recombinant TSG-6 to Hylan-B and SubsequentTransfer of Heavy Chains from Inter-α-inhibitor to Hyaluronan inSolution by Hylan-B-TSG-6 Complexes

The goal of this study was to demonstrate that, in addition tohyaluronan (HA) associated with a solid surface, as shown in Example 1,divinylsulfone crosslinked HA, in the form of a hydrated gel asdescribed in U.S. Pat. No. 4,582,865, is also able to form complexeswith TSG-6 protein, and that these HA-TSG-6 complexes can subsequentlyinteract with the plasma protein inter-α-inhibitor (IαI) and transferheavy chains (HC) from IαI to soluble HA that is in contact with the HAgel. In order to demonstrate this ability of a chemically cross-linkedHA-based gel, the HA gel known as Hylan-B was used.

Materials and Methods

Reagents. Hyaluronan lyase from Streptomyces hyalurolyticus andbiotinylated hyaluronan binding protein (HABP-bio) were purchased fromAssociates of Cape Cod. SelectHA™ 30 kDa was purchased from HyaloseL.L.C. Human plasma was obtained from the blood bank of the NYU MedicalCenter. Rabbit anti-human IαI was from Dako. Although this antibody wasraised against 111, it did not detect bikunin in immunoblotting andELISA and is therefore referred to as HC-specific. The rabbit anti-TSG-6antibody was raised against native recombinant TSG-6 and has beendescribed (Mindrescu et al., 2005). Biotinylated goat anti-rabbit Ig wasfrom Dako and streptavidin-alkaline phosphatase conjugate was fromInvitrogen. The alkaline phosphatase substrate was BCIP/NBT from Bio-Radfor immunoblots. PDVF membrane for immunoblotting was from Millipore(Immobilon P). Hylan-B gel was obtained from the Matrix BiologyInstitute (Edgewater, N.J.) as a hydrated gel suspended in dH₂O.

TSG-6 protein. TSG-6 protein was expressed in BTI-TN-5B1-4 insect cellsafter infection with recombinant nuclear polyhedrosis virus(baculovirus) and purified as described (Wisniewski et al., 1994 and2005).

Binding of TSG-6 to Hylan-B gel. Hylan-B gel was stored suspended indH₂O. Before the binding experiment, the gel was washed extensively andequilibrated with TTBS (20 mM Tris pH 7.5, 500 mM NaCl, 0.1% Tween-20).The gel was then incubated with 30 nM of recombinant TSG-6 in TTBS at37° C. for 2 h under constant rotation to facilitate contact of TSG-6with the gel particles. Finally, the gel was washed extensively withTTBS to remove any free TSG-6. In order to test the stability of thebond between. TSG-6 and Hylan-B, one aliquot of gel was then treatedwith 6M guanidine HCl containing 8% of lauryl sulfobetain (LSB). Afterincubation for 30 min at ambient temperature, the gel was washedextensively to remove all dissociated TSG-6 and the guanidine/LSBsolution, and the remaining supernatant was removed by centrifugation ina Spin-X column at 20,000 g for 3 min. The remaining gel was thensubjected to digestion by 50 μl of a 10 u/ml solution of Streptomyceshyaluronan lyase for 2 h at 37° C. The digested gel was collected bycentrifugation in a Spin-X column at 20,000 g for 3 min and analyzed byimmunoblotting using a rabbit anti-TSG-6 antibody.

Transfer of HCs by HA gel-TSG-6 complexes. Hylan-B gel was storedsuspended in dH₂O. Before the binding experiment, the gel was washedextensively and equilibrated with the buffer used for the subsequentbinding of TSG-6 to Hylan B, either TTBS, TBS (20 mM Tris pH 7.5, 500 mMNaCl), PBS 5 mM MgCl₂, or PBS containing 5 mM MgCl₂ and 0.1% Tween-20).The gel was then incubated with 30 nM of recombinant TSG-6 in the samebuffer at 37° C. for 2 h under constant rotation to facilitate contactof TSG-6 with the gel particles. Finally, the gel was washed extensivelywith TTBS to remove any free TSG-6. The washed hylan B gel containingcomplexes with TSG-6 was then incubated with diluted human plasma, as asource of IαI, at a final concentration of 1:500 in the presence ofSelectHA™30 kDa to transfer HCs from IαI to the SelectHA™. Theincubation was carried out in PBS containing 5 mM MgCl₂ to facilitate HCtransfer by HA-TSG-6 complexes in a 2-step reaction (Colon et al.,2009). The supernatant containing the SelectHA™ was then collected andanalyzed by immunoblotting for the presence of HA-HC complexes usingeither a rabbit anti-HC antibody or a HA-specific probe (HABP).Immunoblotting was carried out using 12% polyacrylamide gels anddenaturing conditions (2% SDS, 5% 2-mercaptoethanol), and PVDF asblotting membrane.

Results

Formation of stable Hylan-B-TSG-6 complexes. FIG. 12 shows that TSG-6protein, after incubation with Hylan-B and extensive washing with TTBS,was found associated with Hylan-B (lane 1). Although treatment with 6Mguanidine HCl containing 8% LSB resulted in a significant decrease ofthe amount of TSG-6 associated with the hylan B gel, TSG-6 forming aguanidine-resistant, i.e., stable bond could be detected afterincubation of TSG-6 with Hylan-B (lane 2).

HC transfer by pre-formed Hylan-B-TSG-6 complexes. FIG. 13 shows theformation of water soluble HA-HC complexes, the product of HC transferfrom IαI to HA in solution, after the incubation of pre-formedHylan-B-TSG-6 complexes with Select HA™ in the presence of diluted humanplasma as a source of IαI (lanes 1 to 4). TSG-6 binding to Hylan-B, thefirst step of the reaction, was carried out in either TTBS (lane 1), TBS(lane 2), PBS containing 5 mM MgCl₂ (lane 3), or PBS containing 5 mMMgCl₂ and 0.1% Tween-20 (lane 4). Binding of TSG-6 in all four of thesebuffers resulted in subsequent HC transfer from IαI to SelectHA™ thatwas in contact with the Hylan gel. The HA-HC complex is not detectablein a plasma control (lane 5). In order to confirm the identity of theHA-HC complexes, the same samples were blotted again and analyzed with aHA-specific HABP probe (FIG. 14). As in FIG. 13, the HA-HC complex wasdetected after binding of TSG-6 to Hylan-B in various buffers andincubation with diluted human plasma and SelectHA™ in a secondincubation step (lanes 1 to 4). No complex could be detected in theplasma control (lane 5).

Discussion

The data presented in FIG. 12 show that recombinant TSG-6 binds readilyto Hylan-B gel and also, to a lesser degree, forms a guanidine-resistantbond with this gel. Treatment with 6 M guanidine HCl containing 8% oflauryl sulfobetain has been shown to dissociate most non-covalent bondsbetween hyaluronan and associated proteins (Mason et al., 1982; Tsiganoset al., 1986; and Yoneda et al., 1990). It as also shown in this Examplethat TSG-6 bound to Hylan-B in a first-step binding reaction is able totransfer HCs from IαI to water-soluble SelectHA™ in a subsequent secondstep (FIGS. 13 and 14).

Example 4 Binding of Recombinant TSG-6 to Covalink-HA and Formation of aStable Bond at 4° C.

We have shown earlier that recombinant TSG-6 forms a stable, i.e.,guanidine-resistant bond with surface-associated hyaluronan (HA) at 37°C. but not at 4° C. (Wisniewski et al., 2005). The recombinant proteinused in the previous study had been purified using ion exchangechromatography and gel filtration (Mindrescu et al., 2000). In thisExample, it is demonstrated that recombinant TSG-6 purified by analternative procedure is able to form a stable bond withsurface-associated HA at 4° C.

Materials and Methods

Reagents. Covalink-NH plates were purchased from Nunc, sulfo-NHS fromPierce, and EDC was purchased from Sigma. Bacterial HA used for couplingto Cov-NH was obtained from Lifecore Biomedical. The rabbit anti-TSG-6antibody was raised against native recombinant TSG-6 and has beendescribed (Mindrescu et al., 2005). Biotinylated goat anti-rabbit Ig wasfrom Dako and streptavidin-alkaline phosphatase conjugate was fromInvitrogen. The alkaline phosphatase substrate was p-nitrophenylphosphate was purchased from Sigma.

TSG-6 protein. TSG-6 protein was expressed in BTI-TN-5B1-4 insect cellsafter infection with recombinant nuclear polyhedrosis virus(baculovirus) (Wisniewski et al., 1994) and purified as described(Wisniewski et al., 2005). In short, 100 ml of TSG-6-containing culturesupernatant was mixed with 10 ml of HA-Sepharose and incubated overnightat 4° C. under constant rotation. The HA-Sepharose was washed 8 timeswith cold Tris-buffered saline (TTBS: 20 mM Tris pH 7.5, 500 mM NaCl,0.1% Tween-20) and transferred to a disposable 5 ml column. The columnwas eluted with 2 column volumes of 3 M guanidine HCl at 4° C. and 1 mlfractions were collected. The fractions were analyzed for the presenceof protein by determination of A 280 nm. Fractions containing proteinwere pooled and dialyzed extensively at 4° C. against PBS.

Coupling of HA to Covalink-NH plates. HA was coupled to Covalink-NH(Cov-NH) plates as described (Wisniewski et al., 2005; and Frost et al.,1997). In brief, HA solution containing sulfo-NHS was added to the wellsof Cov-NH plates. After addition of EDC, the plates were incubated for 2h at room temperature and overnight at 4° C. Thereafter, the plates werewashed extensively with 2 M NaCl and blocked with 0.2% casein in TTBS.Covalink plates with surface-coupled HA are referred to as Covalink-HA(Cov-HA).

TSG-6 binding using Covalink-HA. The assay for TSG-6 binding to Cov-HAwas carried out as described (Wisniewski et al., 2005). In short, 10 nMof TSG-6 protein in TTBS was incubated in the wells of Cov-HA or Cov-NHplates (as a control) at 4° C. for 16 h. After incubation with TSG-6protein, Cov-HA or Cov-NH was washed 3 times with TTBS, followed byincubation with a rabbit anti-TSG-6 antiserum (dilution 1:1000 in TTBS),a biotinylated goat anti-rabbit immunoglobulin antibody (dilution 1:1000in TTBS), a streptavidin-alkaline phosphatase conjugate (dilution 1:1000in TTBS), and finally p-nitrophenyl phosphate (2 mg/ml in 50 mM Tris, pH9.5). Between every incubation step with antibodies, etc., the wellswere washed three times with 200 μl of TTBS. The amount ofdephosphorylated substrate was determined by measuring the absorbance(A) at 410 nm, using the wave length of 750 nm as reference. In order totest the stability of the bond between TSG-6 and surface-coupled HA,selected wells were treated with 6M guanidine HCl containing 8% laurylsulfobetain (LSB) for 15 min at ambient temperature, a treatment thatresults in the dissociation of most non-covalent bonds between proteinsand HA (Yoneda et al., 1990).

Results

Formation of a stable HA-TSG-6 complexes. Using recombinant TSG-6,purified by affinity chromatography on HA-Sepharose, it was found thatincubation at 4° C. for 16 h resulted in binding of TSG-6 tosurface-associated HA (Cov-HA) (FIG. 15, lane 2) and in the formation ofa stable, i.e, guanidine-resistant bond (FIG. 15, lane 3). Treatment ofTSG-6 bound to Cov-HA with 6M guanidine HCl containing 8% LSB resultedin the dissociation of some TSG-6, but 75% of the TSG-6 formed aguanidine-resistant, i.e., stable bond with Cov-HA (lane 3 vs. 2). Lane5 of FIG. 15 shows that the non-specific, i.e., HA-independent bindingof TSG-6 to Cov-NH is negligible.

Discussion

We reported earlier that recombinant TSG-6 purified by a protocolincluding ion exchange chromatography and gel filtration, but notaffinity chromatography on immobilized HA, formed a stable, i.e.,guanidine-resistant bond with HA coupled to a solid surface (Wisniewskiet al., 2005), and that formation of the stable bond was strictlytemperature dependent, i.e., the stable bond was formed at 37° C., butnot at 4° C. (Wisniewski et al., 2005). Here, the present inventors areproviding evidence that recombinant TSG-6 purified by affinitychromatography on HA-Sepharose (Wisniewski et al., 2005) is able to formsuch a stable bond at 4° C. The new data presented in this Examplesuggest that binding of native TSG-6 to HA-Sepharose during itspurification by affinity chromatography, or the subsequent elution ofthis protein from the HA-Sepharose with 3M guanidine HCl, or thecombination of both, result in a lasting conformational change enablingTSG-6 to form a stable bond with surface-associated HA at 4° C.

Having now fully described this invention, it will be appreciated bythose skilled in the art that the same can be performed within a widerange of equivalent parameters, concentrations, and conditions withoutdeparting from the spirit and scope of the invention and without undueexperimentation.

While this invention has been described in connection with specificembodiments thereof, it will be understood that it is capable of furthermodifications. This application is intended to cover any variations,uses, or adaptations of the inventions following, in general, theprinciples of the invention and including such departures from thepresent disclosure as come within known or customary practice within theart to which the invention pertains and as may be applied to theessential features hereinbefore set forth as follows in the scope of theappended claims.

All references cited herein, including journal articles or abstracts,published or corresponding U.S. or foreign patent applications, issuedU.S. or foreign patents, or any other references, are entirelyincorporated by reference herein, including all data, tables, figures,and text presented in the cited references. Additionally, the entirecontents of the references cited within the references cited herein arealso entirely incorporated by references.

Reference to known method steps, conventional methods steps, knownmethods or conventional methods is not in any way an admission that anyaspect, description or embodiment of the present invention is disclosed,taught or suggested in the relevant art.

The foregoing description of the specific embodiments will so fullyreveal the general nature of the invention that others can, by applyingknowledge within the skill of the art (including the contents of thereferences cited herein), readily modify and/or adapt for variousapplications such specific embodiments, without undue experimentation,without departing from the general concept of the present invention.Therefore, such adaptations and modifications are intended to be withinthe meaning and range of equivalents of the disclosed embodiments, basedon the teaching and guidance presented herein. It is to be understoodthat the phraseology or terminology herein is for the purpose ofdescription and not of limitation, such that the terminology orphraseology of the present specification is to be interpreted by theskilled artisan in light of the teachings and guidance presented herein,in combination with the knowledge of one of ordinary skill in the art.

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1. A biocompatible material in the form of a solid, a cross-linked gelor liposomes, comprising a stable complex of TNF-stimulated gene 6protein (TSG-6) and hyaluronan (HA), wherein said HA is itself thecross-linked gel or solid, is part of the cross-linked gel, or isattached either to a solid biocompatible or pharmaceutically acceptablecarrier or to a liposome and wherein said TSG-6 in said stable complexis capable of transferring heavy chains (HCs) of inter-α-inhibitor (IαI)to bound or free HA.
 2. The biocompatible material of claim 1, whereinsaid HA in said stable complex of TSG-6 and HA is attached to said solidbiocompatible or pharmaceutically acceptable carrier.
 3. Thebiocompatible material of claim 2, wherein, said solid biocompatible orpharmaceutically acceptable carrier is a nanoparticle.
 4. Thebiocompatible material of claim 1, which is present on the surface of asolid medical device that is implantable or in-dwelling in a patient oris transiently introduced into a patient during the course of a medicalprocedure.
 5. The biocompatible material of claim 1, wherein said HA insaid stable complex of TSG-6 and HA is a cross-linked HA in across-linked HA-containing gel.
 6. The biocompatible material of claim1, wherein said HA is a solid dry powder of cross-linked HA or of across-linked mixed polymer of HA and at least one other polymer, whichwhen hydrated with a solution containing TSG-6, forms a cross-linked HAor cross-linked HA-containing gel in which TSG-6 is in a stable complexwith the HA.
 7. The biocompatible material of claim 1, wherein said HAin said stable complex of TSG-6 and HA is attached to a liposome.
 8. Thebiocompatible material of claim 1, which is biodegradable.
 9. Thebiocompatible material of claim 1, wherein said stable complex of TSG-6and HA is capable of being released in a soluble form.
 10. A solublestable complex of TSG-6 and HA that is released from the biocompatiblematerial of claim
 9. 11. In a method for using a biocompatible material,in the form of a hyaluronan (HA) attached to a solid or a liposome, orcross-linked in a cross-linked HA or cross-linked HA-containing gel, totreat a disease, disorder or condition for which the biocompatiblematerial is effective, the improvement wherein the HA is stablycomplexed with TNF-stimulated gene 6 protein (TSG-6).
 12. A method forlocally inhibiting inflammation, comprising locally introducing thebiocompatible material of claim 1 into a patient in need thereof. 13.The method of claim 12, wherein said biocompatible material is implantedin the patient.
 14. The method of claim 12, wherein said biocompatiblematerial is a cross-linked gel or liposome.